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Lannett Company

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uuid0004oga

Namestring
Lannett Company
Legal namestring
Lannett Company, Inc.
Websiteurl
lannett.com
Company typeenum
Public
Founded yearint
1942
Descriptiontext

Lannett Company, Inc. is a US-based generic pharmaceutical manufacturer founded in 1942 and headquartered in Philadelphia, Pennsylvania. The company develops, manufactures, and distributes over 100 unique pharmaceutical product families spanning cardiovascular, central nervous system, anti-infective, analgesic, and respiratory therapeutic categories, across dosage forms including tablets, capsules, oral solutions, elixirs, syrups, inhalation anesthetics, and nasal sprays. Lannett holds 113 FDA-approved ANDAs, operates a 425,000-square-foot cGMP manufacturing facility in Seymour, Indiana with annual capacity of approximately 3.6 billion dosage units, and conducts additional manufacturing across Pennsylvania, New York, Georgia, New Jersey, Kentucky, Alabama, Puerto Rico, Switzerland, and China through Kremers Urban Pharmaceuticals and other subsidiaries.

The company generates revenue primarily through B2B sales to pharmaceutical wholesale distributors, retail pharmacy chains, hospital systems, and specialty pharmacies across the United States, with a dedicated CDMO platform (lannettcdmo.com) providing contract development and manufacturing services to third-party pharmaceutical partners. Lannett has historically specialized in complex generics and non-opioid controlled substance medications, and most recently received FDA approval in May 2026 for LANGLARA, an interchangeable insulin glargine biosimilar co-developed with subsidiary Lanexa Biologics and Sunshine Lake Pharma. The company is publicly traded (NYSE: LCI; OTC: LCNTF) and is currently being acquired by Aurobindo Pharma USA for approximately $250 million on a cash-free, debt-free basis (5.5x EBITDA), with FTC approval received in June 2026 and closing expected before end of June 2026.

Short descriptiontext

Lannett Company is a US generic pharmaceutical manufacturer producing over 100 product families across cardiovascular, CNS, anti-infective, analgesic, and respiratory categories. Founded in 1942, the Philadelphia-based company operates seven US manufacturing facilities and is being acquired by Aurobindo Pharma for $250 million.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
501–1,000
akta.pro rankint
HeadquartersPhiladelphia, United States
HQ citystring
Philadelphia
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices19 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
generic pharmaceutical manufacturing, complex generic drugs, controlled substance generics, CDMO services, biosimilar development
Industry2 codes
1Ophthalmic & Otic Generics
CodeHLAIABAFPrimaryYes
2Respiratory & Allergy Pharmaceuticals
CodeHLAIAAAHPrimaryNo
NAICS code2 codes
  • Drugs and Druggists' Sundries Merchant Wholesalers424210
  • Medical, Dental, and Hospital Equipment and Supplies Merchant Wholesalers42345
SIC code2 codes
  • Pharmaceutical Preparations2834
  • Wholesale-Drugs, Proprietaries & Druggists' Sundries5122
Product category
Generic Pharmaceuticals
Social media profiles1 record
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model2 records
1Generic Pharmaceutical Product Sales
TypeOne Time License
Description

Lannett generates revenue through the manufacture and sale of generic pharmaceutical products to pharmacies, healthcare providers, and distribution networks across the United States. The company manufactures over 100 unique pharmaceutical product families spanning multiple therapeutic areas including cardiovascular, central nervous system, anti-infective, analgesic, and respiratory medications. Revenue is generated through direct sales to distributors and healthcare institutions.

businessworld.in
2CDMO (Contract Development and Manufacturing Organization)
TypeProfessional Services
Description

Lannett offers contract development and manufacturing services through its CDMO platform (lannettcdmo.com), providing manufacturing capabilities to other pharmaceutical companies. This represents an additional revenue stream from third-party manufacturing partnerships.

lannett.com
Marketing channels4 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels4 records

Each record includes

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

Cost components6 values
Supply Chain, Personnel, Operations, Technology or R&D, Infrastructure, Marketing or Sales
Pricing details1 tier
1Generic pharmaceuticals are priced at significantly lower costs compared to branded equivalents, providing affordable medication access
ModelUnit PricingBilling cadencePay-as-you-go
Notes

Generic medicines are priced at a fraction of brand-name equivalents, making them more accessible to patients. Lannett does not typically offer patient assistance programs or discount programs, as its core value proposition is providing safe, effective medicines at affordable prices through the standard pharmaceutical supply chain.

lannett.com
GTM typeB2B
B2B
Offering typeHardware or Manufacturing
Hardware or Manufacturing
Brand1 record
1Kremers Urban Pharmaceuticals
Description

Wholly-owned subsidiary of Lannett Company, originally named Kremers Urban Pharmaceuticals, Inc., home to the Seymour, Indiana manufacturing facility.

lannett.com
Core offering1 text field

Lannett Company develops, manufactures, and distributes generic prescription pharmaceutical products in tablet, capsule, liquid, nasal spray, and inhalation anesthetic dosage forms. The company produces over 100 unique pharmaceutical product families spanning cardiovascular, central nervous system, anti-infective, analgesic, and respiratory therapeutic areas, with 113 FDA-approved ANDAs. Lannett also provides CDMO (Contract Development and Manufacturing Organization) services through a dedicated platform and recently received FDA approval for LANGLARA, an interchangeable insulin glargine biosimilar.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 4 values shown
  • 113 approved ANDAs provide substantial regulatory asset base
+3 more records
Product overview1 text field

Lannett Company is a generic pharmaceutical manufacturer offering a diverse portfolio of over 100 unique pharmaceutical product families across multiple dosage forms including tablets, capsules, liquids, syrups, elixirs, sprays, and inhalation anesthetics. The company's product portfolio spans therapeutic areas such as cardiovascular medications (Verelan PM, Levothyroxine, Mexiletine), central nervous system treatments (Amphetamine Sulfate, Methylphenidate, Oxybutynin), anti-infectives (Azithromycin), and various other therapeutic categories. Lannett also provides CDMO (Contract Development and Manufacturing Organization) services through its dedicated platform, and has recently received FDA approval for LANGLARA, an interchangeable insulin glargine biosimilar developed in partnership with Lanexa Biologics and Sunshine Lake Pharma. Products are manufactured across multiple U.S. facilities in Pennsylvania, Indiana, and New York, with some products also manufactured at international sites.

Product and service13 records
1Verelan PM Capsules
CategoryGeneric Pharmaceutical - Cardiovascular
Description

Extended-release verapamil capsules for cardiovascular treatment, available in 100mg, 200mg, and 300mg dosages. Manufactured at Lannett's Gainesville, Georgia facility.

2Azithromycin Tablets
CategoryGeneric Pharmaceutical - Anti-infective
Description

Immediate-release azithromycin tablets for antibacterial treatment, available in 250mg and 500mg dosages. Manufactured at Lannett's Dongguan, China facility.

3Oxybutynin Tablets
CategoryGeneric Pharmaceutical - CNS
Description

Extended-release oxybutynin chloride tablets for overactive bladder treatment, available in 5mg, 10mg, and 15mg dosages.

4Oxybutynin Syrup
CategoryGeneric Pharmaceutical - CNS
Description

Oxybutynin chloride syrup for overactive bladder treatment, 5mg/5mL dosage with raspberry flavor.

5Hyosyne Elixir
CategoryGeneric Pharmaceutical - Gastrointestinal
Description

Hyoscyamine elixir for gastrointestinal disorders, 0.125mg/5mL dosage with lemon flavor.

6Ferrous Sulfate Elixir
CategoryGeneric Pharmaceutical - Hematology
Description

Ferrous sulfate elixir for iron deficiency anemia treatment, 220mg/5mL with orange-lemon flavor.

7Levorphanol Tartrate Tablets
CategoryGeneric Pharmaceutical - Analgesic
Description

Opioid analgesic tablets for pain management, available in 2mg and 3mg dosages with REMS requirements. Manufactured at East Windsor, New Jersey facility.

8Levothyroxine Tablets
CategoryGeneric Pharmaceutical - Endocrine
Description

Levothyroxine sodium tablets for thyroid hormone replacement, available in multiple strengths from 25mcg to 300mcg. Manufactured at Caguas, Puerto Rico facility.

9Mexiletine Capsules
CategoryGeneric Pharmaceutical - Cardiovascular
Description

Antiarrhythmic capsules for ventricular arrhythmia treatment, available in 150mg, 200mg, and 250mg dosages. Manufactured at Manno, Switzerland facility.

10Amphetamine Sulfate Tablets
CategoryGeneric Pharmaceutical - CNS/Controlled Substance
Description

Immediate-release amphetamine sulfate tablets for ADHD and narcolepsy treatment, available in 5mg and 10mg dosages. Manufactured at Hoschton, Georgia facility.

11LANGLARA (Insulin Glargine Biosimilar)
CategoryBiosimilar - Diabetes
Description

FDA-approved interchangeable biosimilar referencing Sanofi's Lantus (insulin glargine) for diabetes treatment. Developed jointly by Lannett Company, its subsidiary Lanexa Biologics, and Sunshine Lake Pharma. Can be substituted for Lantus at pharmacies without prescriber intervention in states permitting such substitution.

12CDMO Services
CategoryContract Manufacturing Services
Description

Contract development and manufacturing organization services for pharmaceutical products, providing manufacturing capabilities to other pharmaceutical companies for solid and liquid dosage forms through the dedicated platform at lannettcdmo.com.

13Mycophenolate Mofetil for Oral Suspension
CategoryGeneric Pharmaceutical - Immunosuppressant
Description

Mycophenolate mofetil oral suspension (immunosuppressant), 200 mg/mL. Received first-cycle FDA approval, representing a new dosage form for Lannett (powder for oral suspension).

Scale indicator8 records

Each record includes

Type, Value, Description, Source

Partnership3 partners
Strategic tierMinorTypeOthersAnnounced on2026-06-18
Description

As a condition of FTC approval for Aurobindo Pharma's acquisition of Lannett, Lannett (via Aurobindo) is required to divest four generic drug products to Quagen Pharmaceuticals LLC. The divestiture includes mycophenolate mofetil oral suspension, niacin extended release tablets, pilocarpine tablets, and rabeprazole sodium delayed release tablets. Both Aurobindo and Lannett must provide transition services to enable Quagen to operate the divested assets.

2Lanexa Biologics
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-05-04
Description

Lannett Company, through its subsidiary Lanexa Biologics, jointly developed LANGLARA (insulin glargine-aldy), an interchangeable biosimilar referencing Sanofi Lantus, with co-development partner Sunshine Lake Pharma. Lannett and Lanexa Biologics intend to pursue broad formulary placement across commercial channels, leveraging each partner's manufacturing and commercialization capabilities.

businesswire.com
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-05-04
Description

Sunshine Lake Pharma partnered with Lannett Company and its subsidiary Lanexa Biologics to co-develop LANGLARA, an FDA-approved interchangeable insulin glargine biosimilar. Sunshine Lake Pharma leverages its large-scale biologics manufacturing capabilities to supply the US market with the biosimilar product.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers5 records
TypeDirect peer
TypeBroad incumbent
Description

Global generic and biosimilar leader with operations in cardiovascular, CNS, anti-infective, and respiratory categories overlapping Lannett's portfolio. CCO Maureen Cavanaugh previously held senior positions at Sandoz.

TypeDirect peer
Description

Indian pharmaceutical company acquiring Lannett for $250M; one of the largest global generic manufacturers with extensive US presence. The transaction itself highlights direct portfolio and operational overlap between the two companies.

TypeBroad incumbent
Description

World's largest generic drug manufacturer with a broad portfolio across virtually all therapeutic areas where Lannett competes. Multiple Lannett executives (Crew, Cavanaugh, Abt, Brock) previously held senior roles at Teva, making it the most directly comparable peer in scale and portfolio breadth.

TypeBroad incumbent
Description

Large-scale generic pharmaceutical manufacturer with a diversified portfolio across most therapeutic categories and significant US manufacturing presence, directly overlapping Lannett's product and customer footprint.

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 risks6 records

Each record includes

Headline, Details, Source

Key highlights6 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers3 records

Each record includes

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

Segment4 records

Each record includes

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

Ideal customer profile2 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
No
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature3 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles14 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

Subsidiaries1 record

Each record includes

Name, Acquired on, Relationship type, Type, Business focus

No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds2 records

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&A3 records

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 →

Lannett Company

Generic Pharmaceuticalslannett.com

Lannett Company is a US generic pharmaceutical manufacturer producing over 100 product families across cardiovascular, CNS, anti-infective, analgesic, and respiratory categories. Founded in 1942, the Philadelphia-based company operates seven US manufacturing facilities and is being acquired by Aurobindo Pharma for $250 million.

What Lannett Company does

Lannett Company, Inc. is a US-based generic pharmaceutical manufacturer founded in 1942 and headquartered in Philadelphia, Pennsylvania. The company develops, manufactures, and distributes over 100 unique pharmaceutical product families spanning cardiovascular, central nervous system, anti-infective, analgesic, and respiratory therapeutic categories, across dosage forms including tablets, capsules, oral solutions, elixirs, syrups, inhalation anesthetics, and nasal sprays. Lannett holds 113 FDA-approved ANDAs, operates a 425,000-square-foot cGMP manufacturing facility in Seymour, Indiana with annual capacity of approximately 3.6 billion dosage units, and conducts additional manufacturing across Pennsylvania, New York, Georgia, New Jersey, Kentucky, Alabama, Puerto Rico, Switzerland, and China through Kremers Urban Pharmaceuticals and other subsidiaries.

The company generates revenue primarily through B2B sales to pharmaceutical wholesale distributors, retail pharmacy chains, hospital systems, and specialty pharmacies across the United States, with a dedicated CDMO platform (lannettcdmo.com) providing contract development and manufacturing services to third-party pharmaceutical partners. Lannett has historically specialized in complex generics and non-opioid controlled substance medications, and most recently received FDA approval in May 2026 for LANGLARA, an interchangeable insulin glargine biosimilar co-developed with subsidiary Lanexa Biologics and Sunshine Lake Pharma. The company is publicly traded (NYSE: LCI; OTC: LCNTF) and is currently being acquired by Aurobindo Pharma USA for approximately $250 million on a cash-free, debt-free basis (5.5x EBITDA), with FTC approval received in June 2026 and closing expected before end of June 2026.

Lannett Company firmographics

Firmographics
Name
Lannett Company
Legal name
Lannett Company, Inc.
Website
https://lannett.com
Company type
Public
Founded year
1942
Operating status
Operating
Headcount range
501–1,000 employees
Short description
Lannett Company is a US generic pharmaceutical manufacturer producing over 100 product families across cardiovascular, CNS, anti-infective, analgesic, and respiratory categories. Founded in 1942, the Philadelphia-based company operates seven US manufacturing facilities and is being acquired by Aurobindo Pharma for $250 million.
Ownership category
akta.pro rank

Lannett Company industry classification

Industry
Product category
Generic Pharmaceuticals
NAICS
Drugs and Druggists' Sundries Merchant Wholesalers (424210), Medical, Dental, and Hospital Equipment and Supplies Merchant Wholesalers (42345)
SIC
Pharmaceutical Preparations (2834), Wholesale-Drugs, Proprietaries & Druggists' Sundries (5122)
akta.pro primary industry
Ophthalmic & Otic Generics (HLAIABAF)
akta.pro secondary industry
Respiratory & Allergy Pharmaceuticals (HLAIAAAH)

Keywords

  • Generic pharmaceutical manufacturing
  • Complex generic drugs
  • Controlled substance generics
  • CDMO services
  • Biosimilar development

Where Lannett Company is headquartered

Location

Headquarters

HQ city
Philadelphia
HQ country
United States
HQ region
North America

Offices19 records

Markets served

Lannett Company business model

Business model
GTM type
B2B
Offering type
Hardware or Manufacturing
Cost components
Supply Chain, Personnel, Operations, Technology or R&D, Infrastructure, Marketing or Sales

Revenue model

  1. Generic Pharmaceutical Product Sales: Lannett generates revenue through the manufacture and sale of generic pharmaceutical products to pharmacies, healthcare providers, and distribution networks across the United States. The company manufactures over 100 unique pharmaceutical product families spanning multiple therapeutic areas including cardiovascular, central nervous system, anti-infective, analgesic, and respiratory medications. Revenue is generated through direct sales to distributors and healthcare institutions.
  2. CDMO (Contract Development and Manufacturing Organization): Lannett offers contract development and manufacturing services through its CDMO platform (lannettcdmo.com), providing manufacturing capabilities to other pharmaceutical companies. This represents an additional revenue stream from third-party manufacturing partnerships.

Pricing tiers

ModelBillingPrice
Unit PricingPay-as-you-goGeneric pharmaceuticals are priced at significantly lower costs compared to branded equivalents, providing affordable medication access

Go-to-market motion1 record

Distribution channels4 records

Marketing channels4 records

Lannett Company product offering

Product offering

Core offering

Lannett Company develops, manufactures, and distributes generic prescription pharmaceutical products in tablet, capsule, liquid, nasal spray, and inhalation anesthetic dosage forms. The company produces over 100 unique pharmaceutical product families spanning cardiovascular, central nervous system, anti-infective, analgesic, and respiratory therapeutic areas, with 113 FDA-approved ANDAs. Lannett also provides CDMO (Contract Development and Manufacturing Organization) services through a dedicated platform and recently received FDA approval for LANGLARA, an interchangeable insulin glargine biosimilar.

Product overview

Lannett Company is a generic pharmaceutical manufacturer offering a diverse portfolio of over 100 unique pharmaceutical product families across multiple dosage forms including tablets, capsules, liquids, syrups, elixirs, sprays, and inhalation anesthetics. The company's product portfolio spans therapeutic areas such as cardiovascular medications (Verelan PM, Levothyroxine, Mexiletine), central nervous system treatments (Amphetamine Sulfate, Methylphenidate, Oxybutynin), anti-infectives (Azithromycin), and various other therapeutic categories. Lannett also provides CDMO (Contract Development and Manufacturing Organization) services through its dedicated platform, and has recently received FDA approval for LANGLARA, an interchangeable insulin glargine biosimilar developed in partnership with Lanexa Biologics and Sunshine Lake Pharma. Products are manufactured across multiple U.S. facilities in Pennsylvania, Indiana, and New York, with some products also manufactured at international sites.

Differentiator

Problem solved

Functional benefit

Brands

  • Kremers Urban Pharmaceuticals: Wholly-owned subsidiary of Lannett Company, originally named Kremers Urban Pharmaceuticals, Inc., home to the Seymour, Indiana manufacturing facility.

Products and services

  • Verelan PM Capsules Extended-release verapamil capsules for cardiovascular treatment, available in 100mg, 200mg, and 300mg dosages. Manufactured at Lannett's Gainesville, Georgia facility.
  • Azithromycin Tablets Immediate-release azithromycin tablets for antibacterial treatment, available in 250mg and 500mg dosages. Manufactured at Lannett's Dongguan, China facility.
  • Oxybutynin Tablets Extended-release oxybutynin chloride tablets for overactive bladder treatment, available in 5mg, 10mg, and 15mg dosages.
  • Oxybutynin Syrup Oxybutynin chloride syrup for overactive bladder treatment, 5mg/5mL dosage with raspberry flavor.
  • Hyosyne Elixir Hyoscyamine elixir for gastrointestinal disorders, 0.125mg/5mL dosage with lemon flavor.
  • Ferrous Sulfate Elixir Ferrous sulfate elixir for iron deficiency anemia treatment, 220mg/5mL with orange-lemon flavor.
  • Levorphanol Tartrate Tablets Opioid analgesic tablets for pain management, available in 2mg and 3mg dosages with REMS requirements. Manufactured at East Windsor, New Jersey facility.
  • Levothyroxine Tablets Levothyroxine sodium tablets for thyroid hormone replacement, available in multiple strengths from 25mcg to 300mcg. Manufactured at Caguas, Puerto Rico facility.
  • Mexiletine Capsules Antiarrhythmic capsules for ventricular arrhythmia treatment, available in 150mg, 200mg, and 250mg dosages. Manufactured at Manno, Switzerland facility.
  • Amphetamine Sulfate Tablets Immediate-release amphetamine sulfate tablets for ADHD and narcolepsy treatment, available in 5mg and 10mg dosages. Manufactured at Hoschton, Georgia facility.
  • LANGLARA (Insulin Glargine Biosimilar) FDA-approved interchangeable biosimilar referencing Sanofi's Lantus (insulin glargine) for diabetes treatment. Developed jointly by Lannett Company, its subsidiary Lanexa Biologics, and Sunshine Lake Pharma. Can be substituted for Lantus at pharmacies without prescriber intervention in states permitting such substitution.
  • CDMO Services Contract development and manufacturing organization services for pharmaceutical products, providing manufacturing capabilities to other pharmaceutical companies for solid and liquid dosage forms through the dedicated platform at lannettcdmo.com.
  • Mycophenolate Mofetil for Oral Suspension Mycophenolate mofetil oral suspension (immunosuppressant), 200 mg/mL. Received first-cycle FDA approval, representing a new dosage form for Lannett (powder for oral suspension).

Quantifiable outcome

  • 113 approved ANDAs provide substantial regulatory asset base
  • +3 more outcomes

Companies that use Lannett Company

Customer profile

Named customers3 records

Segments4 records

Ideal customer profiles2 records

Lannett Company technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature3 records

Lannett Company partnerships and signals

Strategic signal

Partnerships

Three partnerships are on record, tiered minor and core.

  • Quagen Pharmaceuticals LLCminorOthers · 18 June 2026As a condition of FTC approval for Aurobindo Pharma's acquisition of Lannett, Lannett (via Aurobindo) is required to divest four generic drug products to Quagen Pharmaceuticals LLC. The divestiture includes mycophenolate mofetil oral suspension, niacin extended release tablets, pilocarpine tablets, and rabeprazole sodium delayed release tablets. Both Aurobindo and Lannett must provide transition services to enable Quagen to operate the divested assets.
  • Lanexa BiologicscoreStrategic or Co-development Partner · 4 May 2026Lannett Company, through its subsidiary Lanexa Biologics, jointly developed LANGLARA (insulin glargine-aldy), an interchangeable biosimilar referencing Sanofi Lantus, with co-development partner Sunshine Lake Pharma. Lannett and Lanexa Biologics intend to pursue broad formulary placement across commercial channels, leveraging each partner's manufacturing and commercialization capabilities.
  • Sunshine Lake PharmacoreStrategic or Co-development Partner · 4 May 2026Sunshine Lake Pharma partnered with Lannett Company and its subsidiary Lanexa Biologics to co-develop LANGLARA, an FDA-approved interchangeable insulin glargine biosimilar. Sunshine Lake Pharma leverages its large-scale biologics manufacturing capabilities to supply the US market with the biosimilar product.

Scale indicators8 records

Recent moves6 records

Expansion highlights6 records

Lannett Company competitors and assessment

Company assessment

Direct peers

  • Amneal Pharmaceuticals:
  • Aurobindo Pharma: Indian pharmaceutical company acquiring Lannett for $250M; one of the largest global generic manufacturers with extensive US presence. The transaction itself highlights direct portfolio and operational overlap between the two companies.

Broad incumbents

  • Sandoz (Novartis): Global generic and biosimilar leader with operations in cardiovascular, CNS, anti-infective, and respiratory categories overlapping Lannett's portfolio. CCO Maureen Cavanaugh previously held senior positions at Sandoz.
  • Teva Pharmaceutical Industries: World's largest generic drug manufacturer with a broad portfolio across virtually all therapeutic areas where Lannett competes. Multiple Lannett executives (Crew, Cavanaugh, Abt, Brock) previously held senior roles at Teva, making it the most directly comparable peer in scale and portfolio breadth.
  • Viatris (formerly Mylan/Upjohn): Large-scale generic pharmaceutical manufacturer with a diversified portfolio across most therapeutic categories and significant US manufacturing presence, directly overlapping Lannett's product and customer footprint.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat5 records

Key risks6 records

Key highlights6 records

Customer concentration

Lannett Company social profiles

Digital presence

Lannett Company financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Lannett Company leadership team

Management profile

Number of profiles

Profiles14 records

Lannett Company subsidiaries and ownership

Company hierarchy

Subsidiaries1 record

Lannett Company funding detail

Funding detail

Funding overview

Funding rounds2 records

Investors

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

Lannett Company M&A and investment

M&A and investment

M&A3 records

Investments

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

Frequently asked questions about Lannett Company

What does Lannett Company do?

Lannett Company develops, manufactures, and distributes generic prescription pharmaceutical products in tablet, capsule, liquid, nasal spray, and inhalation anesthetic dosage forms. The company produces over 100 unique pharmaceutical product families spanning cardiovascular, central nervous system, anti-infective, analgesic, and respiratory therapeutic areas, with 113 FDA-approved ANDAs. Lannett also provides CDMO (Contract Development and Manufacturing Organization) services through a dedicated platform and recently received FDA approval for LANGLARA, an interchangeable insulin glargine biosimilar.

Is Lannett Company a public or private company?

Lannett Company is a public company. It is classified as public and is currently operating.

When was Lannett Company founded?

Lannett Company was founded in 1942. It employs 501 to 1,000 people.

Where is Lannett Company based?

Lannett Company is headquartered in Philadelphia, United States, in the North America region.

How does Lannett Company make money?

Two revenue lines are on record. Generic Pharmaceutical Product Sales are the primary driver. The others are CDMO (Contract Development and Manufacturing Organization).

Who are Lannett Company's main competitors?

Direct peers on record are Amneal Pharmaceuticals and Aurobindo Pharma. Broad incumbents are Sandoz (Novartis), Teva Pharmaceutical Industries and Viatris (formerly Mylan/Upjohn).

Does Lannett Company have an API?

No public API is recorded for Lannett Company.

What industry is Lannett Company in?

Lannett Company's product category is Generic Pharmaceuticals. Its primary akta.pro industry code is HLAIABAF, Ophthalmic & Otic Generics, with a secondary code of HLAIAAAH, Respiratory & Allergy Pharmaceuticals. Its NAICS code is 424210 and its SIC code is 2834.

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Live signals
Drug Store NewsLannett launches generic Advair DiskusLannett, a subsidiary of Aurobindo Pharma USA, launched a generic of GSK's Advair Diskus in 100/50 mcg and 250/50 mcg strengths. The launch marks the first product from its inhalation pipeline to be commercialized in the United States. The combination therapy is indicated for asthma and chronic obstructive pulmonary disease.The Times of IndiaAurobindo launches generic copy of asthma therapy Advair in USAurobindo Pharma's subsidiary Lannett launched a generic version of Advair Diskus in the US, a bioequivalent of GSK's Seretide for asthma and COPD. The launch opens an estimated $900 million commercial opportunity and marks Aurobindo's first US inhalation product, pitting it against Cipla. The company aims to reach $2 billion annual US revenue after its $250 million Lannett acquisition.BusinessLineAurobindo’s arm, Lannett company, launches generic version of Advair Diskus in USLannett Company LLC, an arm of Hyderabad-based Aurobindo Pharma, launched a generic version of GSK's Advair Diskus inhalation powder in the US market, combining fluticasone propionate and salmeterol. The company said it is the first product from its inhalation pipeline to be commercialised in the US.ScanXAurobindo launches generic Advair Diskus in US marketAurobindo Pharma's subsidiary Lannett Company LLC launched a generic version of Advair Diskus in the US on August 31, 2026, in 100/50 mcg and 250/50 mcg strengths. It is the company's first commercial inhalation product, targeting asthma and COPD patients. The report does not disclose pricing, sales figures, or regulatory approval details.The HinduAurobindo arm Lannett’s facility in U.S. gets 4 U.S. FDA observationsThe U.S. FDA issued four observations to Lannett Company LLC, a U.S. subsidiary of Aurobindo Pharma, following a routine inspection of its Seymour, Indiana manufacturing facility from August 17 to 21. Aurobindo described the observations as procedural and said it responded within the required timeline. The facility can scale to about 4 billion doses annually.The Times of IndiaUSFDA ends inspection of Aurobindo Pharma arm's facility with 4 observationsThe US Food and Drug Administration concluded a routine inspection of Lannett Company LLC's facility in Seymour, USA, issuing four procedural observations. Aurobindo Pharma, the parent company of Lannett, stated it will respond to these findings within the stipulated timeline while maintaining its commitment to quality standards.BusinessLineAurobindo arm’s facility in US gets 4 observations from USFDAThe USFDA concluded a routine inspection at Lannett Company LLC, a subsidiary of Aurobindo Pharma, resulting in four procedural observations. Aurobindo Pharma stated it will respond to the regulatory body within the stipulated timeline and reaffirmed its commitment to quality standards.MintAurobindo Pharma US subsidiary Lannett Company LLC faces 4 observations from the USFDAAurobindo Pharma reported that its US subsidiary, Lannett Company LLC, received four procedural observations from the US FDA following a routine inspection in August 2026. The company also disclosed that its Indian subsidiary, AuroPeptides Ltd, received one observation regarding facility maintenance during a separate inspection at the same time.The Times of IndiaUSFDA ends inspection of Aurobindo Pharma arm's facility with 4 observationsAurobindo Pharma announced that the USFDA concluded a routine inspection of its subsidiary Lannett Company LLC's facility in Seymour, USA, resulting in four procedural observations. The company stated it will respond to the regulator within the stipulated timeline while maintaining its commitment to quality and compliance standards.Investing.comAurobindo Q1 FY27 slides: revenue up 16%, biosimilars pipeline advances By Investing.comAurobindo Pharma reported a 16.3% year-over-year increase in Q1 FY27 consolidated revenue to INR 9,150 crore, driven by strong performance across its US, Europe, and Growth Markets segments alongside a 25.2% surge in net profit. The company also advanced its strategic initiatives, including the completion of the Lannett acquisition and progress in its CuraTeQ biosimilars pipeline with imminent US FDA filings expected.