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Janssen Pharmaceuticals

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uuid000658o

Namestring
Janssen Pharmaceuticals
Legal namestring
Janssen Pharmaceuticals, Inc.
Websiteurl
xarelto-us.com
Company typeenum
Private
Founded yearstring
-
Descriptiontext

Janssen Pharmaceuticals, Inc. is a wholly-owned pharmaceutical subsidiary of Johnson & Johnson (NYSE: JNJ) and operates as part of J&J's Innovative Medicine segment. The company's flagship commercial product is XARELTO (rivaroxaban), a direct oral anticoagulant (DOAC) that selectively blocks Factor Xa to reduce clotting risk. XARELTO holds the broadest label among DOACs in the US, covering six adult indications (nonvalvular atrial fibrillation stroke prevention, DVT/PE treatment and recurrence reduction, post-hip/knee replacement prophylaxis, hospital-associated clot prevention, CAD, and PAD) and is also the only DOAC approved for pediatric use from birth to 18 years, including post-Fontan procedure prophylaxis.

The business model is prescription pharmaceutical sales through retail pharmacies, PBMs, hospital systems, and mail-order channels, with patient access supported by the XARELTO withMe savings card, a 30-day trial offer, and the J&J Patient Assistance Program. Revenue mechanics depend on per-prescription volume rather than enterprise contracts, and pricing is not publicly disclosed. The company maintains a Medical Information Center in Titusville, NJ (its listed operating base) and operates through Janssen Pharmaceutica NV in Belgium for international licensing activities.

Beyond XARELTO, Janssen's pipeline and partnered programs include JNJ-1900 (NBTXR3), a hafnium oxide nanoparticle radioenhancer co-developed with Nanobiotix for oncology (Phase 2 CONVERGE in NSCLC, Phase 3 NANORAY-312 in head and neck cancer); botaretigene sparoparvovec, a gene therapy in Phase III LUMEOS for X-linked retinitis pigmentosa with MeiraGTx; and multiple Phase 1-4 multiple myeloma studies. The company is not independently publicly traded and does not disclose standalone revenue, but its regulatory, distribution, and clinical evidence base position it as a major player in the US anticoagulant and broader cardiovascular/oncology markets.

Short descriptiontext

Janssen Pharmaceuticals is a Johnson & Johnson subsidiary that markets XARELTO (rivaroxaban), the leading US direct oral anticoagulant, across six adult and two pediatric indications, with a growing pipeline in oncology and gene therapy via partnerships.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1–10
akta.pro rankint
HeadquartersTitusville, United States
HQ citystring
Titusville
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
prescription pharmaceuticals, anticoagulant therapy, cardiovascular medicine, direct oral anticoagulants, thrombosis treatment
Industry2 codes
1Cardiometabolic Pharmaceuticals (Cardiovascular/Diabetes/Obesity)
CodeHLAIAAAEPrimaryYes
2Cardiology & Vascular Specialty Pharmaceuticals
CodeHLAIACAGPrimaryNo
NAICS code3 codes
  • Pharmaceutical and Medicine Manufacturing32541
  • Pharmaceutical and Medicine Manufacturing3254
  • Pharmaceutical Preparation Manufacturing325412
SIC code1 code
  • Pharmaceutical Preparations2834
Product category
Anticoagulant Pharmaceuticals
No data
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1XARELTO Pharmaceutical Sales
TypeHardware Sales
Description

Prescription pharmaceutical product revenue from XARELTO (rivaroxaban), a direct oral anticoagulant marketed for multiple cardiovascular indications including atrial fibrillation, DVT, PE, CAD, PAD, and post-surgical prophylaxis. The product is distributed through retail pharmacies and healthcare providers via prescription.

xarelto-us.com
Marketing channels4 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels3 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Technology or R&D, Supply Chain, Marketing or Sales, Personnel, Operations
Pricing details3 tiers
1XARELTO withMe Savings Card - Commercially insured patients
ModelSubscriptionBilling cadenceAnnual
Notes

Eligible commercially insured patients may pay as little as $10 for up to a 90-day supply. 90-day prescription reduces cost to approximately $3.33 per month, potentially saving up to $80 per year compared to monthly fills. Maximum program benefit per calendar year applies. Offer subject to change without notice.

xarelto-us.com
2XARELTO Trial Offer
ModelFreemiumBilling cadencePay-as-you-go
Notes

Free 30-day trial supply available for eligible patients with a valid signed 30-day prescription (excluding 10-mg tablet and 1 mg/mL oral suspension). One use per lifetime. Terms expire end of each calendar year.

xarelto-us.com
3Johnson & Johnson Patient Assistance Program
ModelSubscriptionBilling cadenceAnnual
Notes

Free medicine available for uninsured or underinsured patients meeting eligibility requirements including income thresholds. Medicare Part D patients must demonstrate not eligible for Low-Income Subsidy and spend more than 4% of gross annual household income on prescription drugs.

xarelto-us.com
GTM typeB2C
B2C
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 of 3 records shown
1XARELTO withMe
Description

Patient savings and support program for XARELTO medication

xarelto-us.com
+2 more records
Core offering1 text field

Janssen Pharmaceuticals develops, manufactures, and markets prescription pharmaceutical products, with the commercial flagship being XARELTO (rivaroxaban), a direct oral anticoagulant (DOAC) that selectively inhibits Factor Xa. XARELTO is approved for stroke prevention in nonvalvular atrial fibrillation, treatment and prevention of DVT/PE, reduction of cardiovascular events in coronary artery disease (CAD) and peripheral artery disease (PAD), prevention of clots after orthopedic surgery, prevention of clots in hospitalized non-surgical patients, and pediatric DVT/PE treatment and post-Fontan clot prevention. The product is supplied as oral tablets and a 1 mg/mL oral suspension.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 6 values shown
  • Over 96% stroke-free rate in atrial fibrillation patients (3.8% stroke rate vs 4.3% for warfarin)
+5 more records
Product overview1 text field

Janssen Pharmaceuticals, a Johnson & Johnson company, markets XARELTO (rivaroxaban), a prescription blood thinner and direct oral anticoagulant (DOAC). XARELTO is the primary pharmaceutical product in the provided sources, offered in tablet and oral suspension forms for multiple adult and pediatric indications. The product portfolio includes the XARELTO medication itself along with the XARELTO withMe patient support program providing savings cards, trial offers, and cost assistance. XARELTO is indicated across six adult cardiovascular/thrombosis conditions and two pediatric uses, making it the most prescribed DOAC in the US with over 80 million prescriptions.

Product and service3 records
1XARELTO (rivaroxaban) tablets
CategoryAnticoagulant pharmaceutical
Description

XARELTO tablets are a prescription direct oral anticoagulant (DOAC) that selectively blocks Factor Xa, marketed by Janssen Pharmaceuticals for stroke prevention in nonvalvular atrial fibrillation, treatment and prevention of DVT/PE, reduction of cardiovascular events in CAD/PAD when combined with low-dose aspirin, and prevention of clots after hip or knee replacement surgery in adults.

2XARELTO (rivaroxaban) 1 mg/mL oral suspension
CategoryAnticoagulant pharmaceutical (pediatric)
Description

XARELTO oral suspension is a liquid formulation of rivaroxaban at 1 mg/mL designed for pediatric patients, with weight-based color-coded dosing guidance. It is the only DOAC with FDA approval for pediatric use from birth to 18 years for treating and reducing risk of recurrent DVT/PE, and the only DOAC indicated to help prevent blood clots in children with congenital heart disease after the Fontan procedure.

3XARELTO withMe patient support program
CategoryPatient support and access service
Description

XARELTO withMe is a patient access and adherence program operated through Janssen CarePath that helps eligible commercially insured patients pay as little as $10 per 90-day XARELTO fill, provides a free 30-day trial supply for qualifying new prescriptions, offers refill reminders and educational resources, and routes uninsured or underinsured patients to the Johnson & Johnson Patient Assistance Program for free medicine.

Scale indicator6 records

Each record includes

Type, Value, Description, Source

Partnership4 partners
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2023-01-01
Description

Global co-development and commercialization license agreement established in 2023 between Nanobiotix and Janssen Pharmaceutica NV (a Johnson & Johnson company) for JNJ-1900 (NBTXR3), a novel hafnium oxide nanoparticle radioenhancer. Johnson & Johnson is sponsoring the Phase 2 CONVERGE study for stage 3 inoperable non-small cell lung cancer and Phase 3 NANORAY-312 study for head and neck cancer. In October 2025, sponsorship and operational control of the Phase 3 head and neck cancer trial was transferred to Johnson & Johnson.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Collaboration for Botaretigene sparoparvovec, an investigational gene therapy for X-linked retinitis pigmentosa. MeiraGTx received a $50 million milestone payment in February 2024 following initiation of the extension study for the Phase III LUMEOS clinical trial. MeiraGTx is a biopharmaceutical company developing gene therapies for retinal diseases.

Strategic tierMinorTypeStrategic or Co-development Partner
Description

Multiple Myeloma research collaboration. Between April 3-16, 2026, Johnson & Johnson Private Limited and Janssen Research & Development LLC each initiated new clinical studies in multiple myeloma across phases 1-4 as part of the broader pharmaceutical research portfolio.

Strategic tierMinorTypeStrategic or Co-development Partner
Description

Collaboration with Johnson & Johnson in autoimmune disease treatments. Odyssey Therapeutics is developing autoimmune disease treatments including ongoing trials and collaborations with Johnson & Johnson and Terray Therapeutics. J&J collaboration supports Odyssey's pipeline development.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Pfizer is the co-marketer of Eliquis (apixaban) with Bristol-Myers Squibb, the principal DOAC competitor to XARELTO. Both companies compete in the same cardiology/anticoagulant category with overlapping physician call points and payer negotiations.

TypeBroad incumbent
Description

Bayer is the joint developer and ex-U.S. commercializer of XARELTO with Janssen, while also independently operating a large cardiovascular and consumer health portfolio (including Aspirin Cardio). The co-development agreement makes Bayer both a partner and a strategic incumbent in the same therapeutic space.

TypeBroad incumbent
Description

Sanofi operates a large cardiovascular and thrombosis franchise (including Plavix historically and Lovenox/Clexane enoxaparin) that competes in adjacent anticoagulant categories. A broad incumbent comparable to Janssen in therapeutic-area breadth and prescription-driven commercial model.

TypeBroad incumbent
Description

Novartis is a large branded pharmaceutical company with overlapping cardiovascular and specialty medicine portfolios, sharing the same prescription-pharma distribution model and prescriber channels as Janssen. A broad incumbent in the same therapeutic and competitive landscape.

TypeBroad incumbent
Description

AstraZeneca markets Brilinta (ticagrelor) in the cardiovascular/thrombosis space and acquired the Factor Xa inhibitor portfolio via its Alexion/Portola acquisition, giving it a direct DOAC competitive position. A broad incumbent in cardiovascular and related specialty pharma categories.

TypeDirect peer
Description

Daiichi Sankyo markets Lixiana/Savaysa (edoxaban), another direct oral Factor Xa inhibitor approved for stroke prevention in AFib and treatment of DVT/PE. Directly competes in the same DOAC class as XARELTO across overlapping cardiovascular indications.

TypeDirect peer
Description

BMS co-markets Eliquis (apixaban) with Pfizer, the leading direct oral anticoagulant that has overtaken XARELTO in U.S. DOAC revenue and scripts. Direct head-to-head competitor in atrial fibrillation stroke prevention, DVT/PE treatment, and post-surgical prophylaxis.

TypeOthers
Description

Dup-removed; Bayer already listed above as co-developer. If a separate low-dose aspirin comparator is needed, Bayer's Aspirin Cardio is a relevant OTC comparator specifically in the CAD/PAD combination therapy positioning where XARELTO+aspirin competes.

TypeDirect peer
Description

Boehringer Ingelheim markets Pradaxa (dabigatran), the first FDA-approved DOAC and a direct competitor to XARELTO in stroke prevention and DVT/PE treatment. Comparable private, research-driven pharmaceutical company with overlapping anticoagulant franchise.

TypeEmerging player
Description

Anthos Therapeutics is developing abelacimab, a Factor XI inhibitor designed as a next-generation anticoagulant with potentially lower bleeding risk. An emerging player whose anticoagulant pipeline, if approved, would directly challenge the DOAC class (XARELTO, Eliquis, etc.) on safety grounds.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

Each record includes

Headline, Details, Source

Competitive moat5 records

Each record includes

Type, Details

Key risks7 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers7 records

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment7 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile6 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature4 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Janssen Pharmaceuticals

Anticoagulant Pharmaceuticalsxarelto-us.com

Janssen Pharmaceuticals is a Johnson & Johnson subsidiary that markets XARELTO (rivaroxaban), the leading US direct oral anticoagulant, across six adult and two pediatric indications, with a growing pipeline in oncology and gene therapy via partnerships.

What Janssen Pharmaceuticals does

Janssen Pharmaceuticals, Inc. is a wholly-owned pharmaceutical subsidiary of Johnson & Johnson (NYSE: JNJ) and operates as part of J&J's Innovative Medicine segment. The company's flagship commercial product is XARELTO (rivaroxaban), a direct oral anticoagulant (DOAC) that selectively blocks Factor Xa to reduce clotting risk. XARELTO holds the broadest label among DOACs in the US, covering six adult indications (nonvalvular atrial fibrillation stroke prevention, DVT/PE treatment and recurrence reduction, post-hip/knee replacement prophylaxis, hospital-associated clot prevention, CAD, and PAD) and is also the only DOAC approved for pediatric use from birth to 18 years, including post-Fontan procedure prophylaxis.

The business model is prescription pharmaceutical sales through retail pharmacies, PBMs, hospital systems, and mail-order channels, with patient access supported by the XARELTO withMe savings card, a 30-day trial offer, and the J&J Patient Assistance Program. Revenue mechanics depend on per-prescription volume rather than enterprise contracts, and pricing is not publicly disclosed. The company maintains a Medical Information Center in Titusville, NJ (its listed operating base) and operates through Janssen Pharmaceutica NV in Belgium for international licensing activities.

Beyond XARELTO, Janssen's pipeline and partnered programs include JNJ-1900 (NBTXR3), a hafnium oxide nanoparticle radioenhancer co-developed with Nanobiotix for oncology (Phase 2 CONVERGE in NSCLC, Phase 3 NANORAY-312 in head and neck cancer); botaretigene sparoparvovec, a gene therapy in Phase III LUMEOS for X-linked retinitis pigmentosa with MeiraGTx; and multiple Phase 1-4 multiple myeloma studies. The company is not independently publicly traded and does not disclose standalone revenue, but its regulatory, distribution, and clinical evidence base position it as a major player in the US anticoagulant and broader cardiovascular/oncology markets.

Janssen Pharmaceuticals firmographics

Firmographics
Name
Janssen Pharmaceuticals
Legal name
Janssen Pharmaceuticals, Inc.
Website
https://xarelto-us.com
Company type
Private
Operating status
Operating
Headcount range
1–10 employees
Short description
Janssen Pharmaceuticals is a Johnson & Johnson subsidiary that markets XARELTO (rivaroxaban), the leading US direct oral anticoagulant, across six adult and two pediatric indications, with a growing pipeline in oncology and gene therapy via partnerships.
Ownership category
akta.pro rank

Janssen Pharmaceuticals industry classification

Industry
Product category
Anticoagulant Pharmaceuticals
NAICS
Pharmaceutical and Medicine Manufacturing (32541), Pharmaceutical and Medicine Manufacturing (3254), Pharmaceutical Preparation Manufacturing (325412)
SIC
Pharmaceutical Preparations (2834)
akta.pro primary industry
Cardiometabolic Pharmaceuticals (Cardiovascular/Diabetes/Obesity) (HLAIAAAE)
akta.pro secondary industry
Cardiology & Vascular Specialty Pharmaceuticals (HLAIACAG)

Keywords

  • Prescription pharmaceuticals
  • Anticoagulant therapy
  • Cardiovascular medicine
  • Direct oral anticoagulants
  • Thrombosis treatment

Where Janssen Pharmaceuticals is headquartered

Location

Headquarters

HQ city
Titusville
HQ country
United States
HQ region
North America

Offices1 record

Markets served

Janssen Pharmaceuticals business model

Business model
GTM type
B2C
Offering type
Hardware or Manufacturing
Cost components
Technology or R&D, Supply Chain, Marketing or Sales, Personnel, Operations

Revenue model

  1. XARELTO Pharmaceutical Sales: Prescription pharmaceutical product revenue from XARELTO (rivaroxaban), a direct oral anticoagulant marketed for multiple cardiovascular indications including atrial fibrillation, DVT, PE, CAD, PAD, and post-surgical prophylaxis. The product is distributed through retail pharmacies and healthcare providers via prescription.

Pricing tiers

ModelBillingPrice
SubscriptionAnnualXARELTO withMe Savings Card - Commercially insured patients
FreemiumPay-as-you-goXARELTO Trial Offer
SubscriptionAnnualJohnson & Johnson Patient Assistance Program

Go-to-market motion1 record

Distribution channels3 records

Marketing channels4 records

Janssen Pharmaceuticals product offering

Product offering

Core offering

Janssen Pharmaceuticals develops, manufactures, and markets prescription pharmaceutical products, with the commercial flagship being XARELTO (rivaroxaban), a direct oral anticoagulant (DOAC) that selectively inhibits Factor Xa. XARELTO is approved for stroke prevention in nonvalvular atrial fibrillation, treatment and prevention of DVT/PE, reduction of cardiovascular events in coronary artery disease (CAD) and peripheral artery disease (PAD), prevention of clots after orthopedic surgery, prevention of clots in hospitalized non-surgical patients, and pediatric DVT/PE treatment and post-Fontan clot prevention. The product is supplied as oral tablets and a 1 mg/mL oral suspension.

Product overview

Janssen Pharmaceuticals, a Johnson & Johnson company, markets XARELTO (rivaroxaban), a prescription blood thinner and direct oral anticoagulant (DOAC). XARELTO is the primary pharmaceutical product in the provided sources, offered in tablet and oral suspension forms for multiple adult and pediatric indications. The product portfolio includes the XARELTO medication itself along with the XARELTO withMe patient support program providing savings cards, trial offers, and cost assistance. XARELTO is indicated across six adult cardiovascular/thrombosis conditions and two pediatric uses, making it the most prescribed DOAC in the US with over 80 million prescriptions.

Differentiator

Problem solved

Functional benefit

Brands

  • XARELTO withMe: Patient savings and support program for XARELTO medication
  • JNJ-1900 (NBTXR3)
  • Botaretigene sparoparvovec

Products and services

  • XARELTO (rivaroxaban) tablets XARELTO tablets are a prescription direct oral anticoagulant (DOAC) that selectively blocks Factor Xa, marketed by Janssen Pharmaceuticals for stroke prevention in nonvalvular atrial fibrillation, treatment and prevention of DVT/PE, reduction of cardiovascular events in CAD/PAD when combined with low-dose aspirin, and prevention of clots after hip or knee replacement surgery in adults.
  • XARELTO (rivaroxaban) 1 mg/mL oral suspension XARELTO oral suspension is a liquid formulation of rivaroxaban at 1 mg/mL designed for pediatric patients, with weight-based color-coded dosing guidance. It is the only DOAC with FDA approval for pediatric use from birth to 18 years for treating and reducing risk of recurrent DVT/PE, and the only DOAC indicated to help prevent blood clots in children with congenital heart disease after the Fontan procedure.
  • XARELTO withMe patient support program XARELTO withMe is a patient access and adherence program operated through Janssen CarePath that helps eligible commercially insured patients pay as little as $10 per 90-day XARELTO fill, provides a free 30-day trial supply for qualifying new prescriptions, offers refill reminders and educational resources, and routes uninsured or underinsured patients to the Johnson & Johnson Patient Assistance Program for free medicine.

Quantifiable outcome

  • Over 96% stroke-free rate in atrial fibrillation patients (3.8% stroke rate vs 4.3% for warfarin)
  • +5 more outcomes

Companies that use Janssen Pharmaceuticals

Customer profile

Named customers7 records

Segments7 records

Ideal customer profiles6 records

Janssen Pharmaceuticals technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature4 records

Janssen Pharmaceuticals partnerships and signals

Strategic signal

Partnerships

Four partnerships are on record, tiered core and minor.

  • NanobiotixcoreStrategic or Co-development Partner · 1 January 2023Global co-development and commercialization license agreement established in 2023 between Nanobiotix and Janssen Pharmaceutica NV (a Johnson & Johnson company) for JNJ-1900 (NBTXR3), a novel hafnium oxide nanoparticle radioenhancer. Johnson & Johnson is sponsoring the Phase 2 CONVERGE study for stage 3 inoperable non-small cell lung cancer and Phase 3 NANORAY-312 study for head and neck cancer. In October 2025, sponsorship and operational control of the Phase 3 head and neck cancer trial was transferred to Johnson & Johnson.
  • MeiraGTxcoreStrategic or Co-development PartnerCollaboration for Botaretigene sparoparvovec, an investigational gene therapy for X-linked retinitis pigmentosa. MeiraGTx received a $50 million milestone payment in February 2024 following initiation of the extension study for the Phase III LUMEOS clinical trial. MeiraGTx is a biopharmaceutical company developing gene therapies for retinal diseases.
  • Johnson & Johnson Private LimitedminorStrategic or Co-development PartnerMultiple Myeloma research collaboration. Between April 3-16, 2026, Johnson & Johnson Private Limited and Janssen Research & Development LLC each initiated new clinical studies in multiple myeloma across phases 1-4 as part of the broader pharmaceutical research portfolio.
  • Odyssey TherapeuticsminorStrategic or Co-development PartnerCollaboration with Johnson & Johnson in autoimmune disease treatments. Odyssey Therapeutics is developing autoimmune disease treatments including ongoing trials and collaborations with Johnson & Johnson and Terray Therapeutics. J&J collaboration supports Odyssey's pipeline development.

Scale indicators6 records

Recent moves6 records

Expansion highlights6 records

Janssen Pharmaceuticals competitors and assessment

Company assessment

Direct peers

  • Pfizer: Pfizer is the co-marketer of Eliquis (apixaban) with Bristol-Myers Squibb, the principal DOAC competitor to XARELTO. Both companies compete in the same cardiology/anticoagulant category with overlapping physician call points and payer negotiations.
  • Daiichi Sankyo: Daiichi Sankyo markets Lixiana/Savaysa (edoxaban), another direct oral Factor Xa inhibitor approved for stroke prevention in AFib and treatment of DVT/PE. Directly competes in the same DOAC class as XARELTO across overlapping cardiovascular indications.
  • Bristol-Myers Squibb: BMS co-markets Eliquis (apixaban) with Pfizer, the leading direct oral anticoagulant that has overtaken XARELTO in U.S. DOAC revenue and scripts. Direct head-to-head competitor in atrial fibrillation stroke prevention, DVT/PE treatment, and post-surgical prophylaxis.
  • Boehringer Ingelheim: Boehringer Ingelheim markets Pradaxa (dabigatran), the first FDA-approved DOAC and a direct competitor to XARELTO in stroke prevention and DVT/PE treatment. Comparable private, research-driven pharmaceutical company with overlapping anticoagulant franchise.

Broad incumbents

  • Bayer: Bayer is the joint developer and ex-U.S. commercializer of XARELTO with Janssen, while also independently operating a large cardiovascular and consumer health portfolio (including Aspirin Cardio). The co-development agreement makes Bayer both a partner and a strategic incumbent in the same therapeutic space.
  • Sanofi: Sanofi operates a large cardiovascular and thrombosis franchise (including Plavix historically and Lovenox/Clexane enoxaparin) that competes in adjacent anticoagulant categories. A broad incumbent comparable to Janssen in therapeutic-area breadth and prescription-driven commercial model.
  • Novartis: Novartis is a large branded pharmaceutical company with overlapping cardiovascular and specialty medicine portfolios, sharing the same prescription-pharma distribution model and prescriber channels as Janssen. A broad incumbent in the same therapeutic and competitive landscape.
  • AstraZeneca: AstraZeneca markets Brilinta (ticagrelor) in the cardiovascular/thrombosis space and acquired the Factor Xa inhibitor portfolio via its Alexion/Portola acquisition, giving it a direct DOAC competitive position. A broad incumbent in cardiovascular and related specialty pharma categories.

Others

  • Bayer (Aspirin Cardio): Dup-removed; Bayer already listed above as co-developer. If a separate low-dose aspirin comparator is needed, Bayer's Aspirin Cardio is a relevant OTC comparator specifically in the CAD/PAD combination therapy positioning where XARELTO+aspirin competes.

Emerging players

  • Anthos Therapeutics: Anthos Therapeutics is developing abelacimab, a Factor XI inhibitor designed as a next-generation anticoagulant with potentially lower bleeding risk. An emerging player whose anticoagulant pipeline, if approved, would directly challenge the DOAC class (XARELTO, Eliquis, etc.) on safety grounds.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat5 records

Key risks7 records

Key highlights7 records

Customer concentration

Janssen Pharmaceuticals financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Janssen Pharmaceuticals leadership team

Management profile

Number of profiles

Janssen Pharmaceuticals funding detail

Funding detail

Funding overview

Funding rounds

Investors

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Janssen Pharmaceuticals M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Janssen Pharmaceuticals

What does Janssen Pharmaceuticals do?

Janssen Pharmaceuticals develops, manufactures, and markets prescription pharmaceutical products, with the commercial flagship being XARELTO (rivaroxaban), a direct oral anticoagulant (DOAC) that selectively inhibits Factor Xa. XARELTO is approved for stroke prevention in nonvalvular atrial fibrillation, treatment and prevention of DVT/PE, reduction of cardiovascular events in coronary artery disease (CAD) and peripheral artery disease (PAD), prevention of clots after orthopedic surgery, prevention of clots in hospitalized non-surgical patients, and pediatric DVT/PE treatment and post-Fontan clot prevention. The product is supplied as oral tablets and a 1 mg/mL oral suspension.

Is Janssen Pharmaceuticals a public or private company?

Janssen Pharmaceuticals is a private company. It is classified as corporate owned and is currently operating.

When was Janssen Pharmaceuticals founded?

Janssen Pharmaceuticals was founded in -1. It employs 1 to 10 people.

Where is Janssen Pharmaceuticals based?

Janssen Pharmaceuticals is headquartered in Titusville, United States, in the North America region.

How does Janssen Pharmaceuticals make money?

One revenue line is on record: XARELTO Pharmaceutical Sales.

Who are Janssen Pharmaceuticals's main competitors?

Direct peers on record are Pfizer, Daiichi Sankyo, Bristol-Myers Squibb and Boehringer Ingelheim. Broad incumbents are Bayer, Sanofi, Novartis and AstraZeneca. Bayer (Aspirin Cardio) is listed as an others. Anthos Therapeutics is listed as an emerging player.

Does Janssen Pharmaceuticals have an API?

No public API is recorded for Janssen Pharmaceuticals.

What industry is Janssen Pharmaceuticals in?

Janssen Pharmaceuticals's product category is Anticoagulant Pharmaceuticals. Its primary akta.pro industry code is HLAIAAAE, Cardiometabolic Pharmaceuticals (Cardiovascular/Diabetes/Obesity), with a secondary code of HLAIACAG, Cardiology & Vascular Specialty Pharmaceuticals. Its NAICS code is 32541 and its SIC code is 2834.

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Live signals
Docwire NewsUsing Wireless Biosensor in Studying Cancer TreatmentsResearchers at Haga Teaching Hospital in the Netherlands will use VitalPatch and pinpointIQ to monitor cancer patients during erythrocyte transfusion, chemotherapy, or immunotherapy. The study, financed by Janssen Pharmaceuticals, aims to identify adverse events and improve treatment management. It began in September 2016 with 30 patients and plans to expand.Psychiatric TimesLumatperone in Adjunctive MDD Treatment: Phase 3 Data and Meta-Analysis FindingsJanssen Pharmaceuticals received FDA approval for lumateperone (Caplyta) as an adjunctive therapy for major depressive disorder, demonstrating reliable clinical response within two to four weeks in patients unresponsive to conventional antidepressants. A network meta-analysis indicates that lumateperone offers a higher likelihood of benefit compared to other newer-generation antipsychotics, supported by a favorable tolerability profile with minimal metabolic and extrapyramidal risks.The National Law ReviewThird Circuit Revives TCPA Class Action for Patient Assistance PrThe Third Circuit Court of Appeals reversed a lower court's dismissal on August 7, 2026, reviving a TCPA class action against Janssen Pharmaceuticals and Johnson & Johnson Health Care Systems over a two-page fax advertising their patient assistance program for the anticoagulant Xarelto. The appellate court held that the fax qualified as an unsolicited advertisement because it promoted the drug's affordability through cost-support messaging, likening it to a coupon that aims to drive brand preference over cheaper alternatives like Warfarin ($20/month vs. $400/month for Xarelto). The court rejected the defendants' argument that adding clinical information pages could neutralize commercial intent, ruling that documents must be read as a whole and that savings messaging constitutes product messaging with profit as its aim.YahooLawmakers must protect, expand Medicare drug cost negotiation | LetterA Medicare patient urges lawmakers to protect and expand the 2022 drug negotiation program, citing a 62% price drop on Xarelto. The Supreme Court rejected six challenges, including Janssen's, and the writer says the courts' decision is a relief. The letter calls for continued legislative support.Business TodayWho is Dr Anil Koul? The scientist PM Modi personally urged to return to IndiaPrime Minister Narendra Modi personally persuaded Dr. Anil Koul, one of India's leading biomedical scientists, to return from Belgium where he was serving as Senior Director and Head of Respiratory Infections Discovery at Johnson & Johnson's Janssen pharmaceutical division. Dr. Koul, who played a crucial role in discovering Bedaquiline—the first new treatment for multidrug-resistant tuberculosis in over four decades—served as Director of CSIR-IMTECH in Chandigarh from 2017 to 2019 before returning to global pharma. In 2025, he joined Bharat Serums & Vaccines and Mankind Pharma as Group Chief Scientific Officer to lead innovation and next-generation drug development in India.BioWorldJanssen Pharmaceutica reports new TMEM175 activatorsJanssen Pharmaceutica identified new activators of the endosomal/lysosomal proton channel TMEM175, which are potentially useful for treating Parkinson's disease. The discovery was reported on June 2, 2026, in a BioWorld Science article.IPWatchdog.comSCOTUS Denies Cert to Pharma Industry Challenges to IRA’s Negotiation Program, USAA’s Section 101 Patent AppealThe U.S. Supreme Court denied certiorari to petitions filed by major pharmaceutical companies, including Janssen, Bristol Myers Squibb, and AstraZeneca, challenging the Medicare drug price negotiation program established by the Inflation Reduction Act. The court also rejected appeals regarding patent eligibility from USAA and a copyright dispute involving Disney. These denials uphold lower court rulings that found no constitutional violations in the government's authority to set drug prices for Medicare coverage.UsnewsUS Supreme Court Rebuffs Pharma Challenge to Biden-Era Drug PriceThe U.S. Supreme Court declined on Monday to hear pharmaceutical industry challenges to a Medicare drug price negotiation plan adopted during the Biden administration, leaving in place lower court decisions that rejected the companies' legal claims. The justices turned away appeals from six major drugmakers—Novo Nordisk, AstraZeneca, Janssen Pharmaceuticals, Bristol Myers Squibb, Novartis, and Boehringer Ingelheim—which argued the plan illegally forces steep discounts and jeopardizes innovation. The Trump administration is defending the program, with CMS Administrator Mehmet Oz citing it as part of efforts to reduce prescription drug costs, and the first negotiated prices on 10 drugs went into effect this year.openPR.comMultiple Myeloma Treatment Pipeline Shows Strong Momentum as 75+ Pharma Companies in the Race | DelveInsightDelveInsight published its 'Multiple Myeloma Pipeline Insights 2026' report covering 75+ pharmaceutical companies developing 80+ pipeline therapies for multiple myeloma, highlighting a robust and active research landscape. Between April 3–16, 2026, six companies — Pfizer, AbbVie, Johnson & Johnson Private Limited, Janssen Research & Development LLC, Hoffmann-La Roche, and Celgene — each initiated new clinical studies in multiple myeloma across phases 1–4. The report also profiles emerging drug candidates such as zevorcabtagene autoleucel (Carsgen Therapeutics), Descartes-08 (Cartesian Therapeutics), GC012F (Gracell Biotechnology), CID-103 (CASI Pharmaceuticals), and STI-1492 (Sorrento Therapeutics), spanning early to mid-stage development.openPR.comJanssen Pharmaceutical "Botaretigene sparoparvovec" Market size expansion of Several Folds by 2034DelveInsight published a market forecast report predicting significant expansion in the market size for Botaretigene sparoparvovec by 2034, an investigational gene therapy developed by Janssen Pharmaceutical for X-linked retinitis pigmentosa. Phase I/II trial data published in the American Journal of Ophthalmology demonstrated improvement in retinal sensitivity and functional vision at 26 and 52 weeks, with no dose-limiting toxicities reported. MeiraGTx received a USD 50 million milestone payment in February 2024 following initiation of the extension study for the Phase III LUMEOS clinical trial.