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Halo Pharmaceutical

Full company profile

uuid0002h1v

Namestring
Halo Pharmaceutical
Legal namestring
Halo Pharma, Inc.
Websiteurl
halopharma.com
Company typeenum
Private
Founded yearint
2002
Descriptiontext

Halo Pharmaceutical is a contract development and manufacturing organization (CDMO) headquartered in Whippany, New Jersey, with primary manufacturing operations at a large-scale facility in Mirabel, Quebec, Canada. Founded in 2002 and historically part of the Noramco Group under SK Capital Partners ownership, the company emerged as a standalone CDMO in May 2026 following SK Capital's sale of Noramco to Siegfried. Halo Pharma provides development, manufacturing, and regulatory support services for solid oral dose, semi-solid, oral liquid, and sterile injectable pharmaceutical products, serving generic and branded pharmaceutical companies with a portfolio that includes 400+ commercial SKUs, 120 active development projects, and more than 90 ANDA/NDA filings to date.

The company's technical platform spans formulation development, analytical method development, validation, tech transfer, commercial manufacturing, and packaging across multiple dosage forms. The Mirabel site holds cGMP registrations with FDA, Health Canada, EMA, ANVISA, and MHRA, and operates under DEA registration for Schedule II-V controlled substances — a regulatory footprint that is uncommon among mid-tier CDMOs. The company has been actively expanding its technological capability, including a $30M+ investment in sterile injectable manufacturing anchored by a new Groninger ready-to-use vial filling line, and the addition of Gerteis dry granulation equipment for solid dose work.

Halo Pharma's business model is project-based contract services revenue: customers pay for development milestones, tech transfer, validation, and commercial manufacturing volumes under multi-year supply agreements. The customer base spans 85+ companies, including Top 10 pharmaceutical and generics players, with a strategic anchor relationship with Apotex covering sterile injectable capacity. Revenue is not publicly disclosed, but operational scale (Mirabel alone employs 200+ staff, with corporate headcount in the 101-250 range) and capital intensity are consistent with a mid-tier diversified CDMO serving both branded and generic pharmaceutical innovators.

Short descriptiontext

Halo Pharmaceutical is a US-headquartered, Canada-manufactured contract development and manufacturing organization (CDMO) serving 85+ generic and branded pharmaceutical clients with solid dose, semi-solid, oral liquid, and sterile injectable products across 400+ commercial SKUs.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
101–250
akta.pro rankint
HeadquartersWhippany, United States
HQ citystring
Whippany
HQ countrystring
United States
HQ regionstring
North America
Markets served

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
pharmaceutical contract manufacturing, drug product development, contract development organization, sterile injectable manufacturing, pharmaceutical formulation services
Industry3 codes
1Small-Molecule Drug Product (Solid/Oral/Parenteral) CDMO
CodeHLAGABABPrimaryYes
2Sterile Fill-Finish & Aseptic Manufacturing CDMO
CodeHLAGABAHPrimaryNo
3Clinical Trial Material (CTM) Manufacturing & Supply CDMO
CodeHLAGABAKPrimaryNo
NAICS code3 codes
  • Pharmaceutical Preparation Manufacturing325412
  • Pharmaceutical and Medicine Manufacturing32541
  • Pharmaceutical and Medicine Manufacturing3254
SIC code2 codes
  • Pharmaceutical Preparations2834
  • Medicinal Chemicals & Botanical Products2833
Product category
Pharmaceutical Contract Development and Manufacturing (CDMO)
Social media profiles1 record
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1Contract Development and Manufacturing Services
TypeProfessional Services
Description

Halo Pharma generates revenue through contract development and manufacturing services for pharmaceutical companies. Services include formulation development, analytical method development, clinical trial material manufacturing, commercial manufacturing, and tech transfer services. Revenue is generated through project-based contracts with pharmaceutical innovators, generics, and OTC companies for development and manufacturing services across solid dose, semi-solid, oral liquid, and sterile formats.

halopharma.com
Marketing channels5 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

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

Cost components6 values
Personnel, Operations, Infrastructure, Technology or R&D, Marketing or Sales, Supply Chain
Pricing details1 tier
1Contract-based development and manufacturing services with custom project pricing
ModelOtherBilling cadenceMulti-year contract
Notes

Services are priced through custom quotes based on project requirements including development phase, dosage form complexity, batch sizes, and regulatory requirements

halopharma.com
GTM typeB2B
B2B
Offering typeServices
Services
Core offering1 text field

Halo Pharma is a contract development and manufacturing organization (CDMO) that provides outsourced formulation development, analytical testing, clinical trial material manufacturing, and commercial-scale production of small molecule drug products. The company serves pharmaceutical innovators, generics manufacturers, and OTC product owners across solid dose, semi-solid, oral liquid, and (in 2026) sterile injectable dosage forms from two North American cGMP facilities in Whippany, NJ and Mirabel, Quebec.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 6 values shown
  • 120 active product development projects supported
+5 more records
Product overview1 text field

Halo Pharma is a contract development and manufacturing organization (CDMO) providing end-to-end pharmaceutical development and manufacturing services. The company operates two North American facilities in Whippany, NJ and Mirabel, Quebec, Canada. Core service modules include Development Services, Analytical Services, Clinical Manufacturing (CTM), Commercial Manufacturing, and Quality Services. These services support manufacturing across multiple dosage forms: Solid Dosage Forms (tablets, capsules, powders), Semi-Solid Dosage Forms (creams, ointments, gels), Oral Liquid Dosage Forms (solutions, suspensions, syrups), and Sterile Injectable Dosage Forms (vials, prefilled syringes, cartridges). The company is expanding into sterile manufacturing in 2026 with a $30+ million investment. An Accelerated Tech Transfer Program offers fixed-price engagements for GMP manufacturing in 16-20 weeks.

Product and service9 records
1Development Services
CategoryDrug Product Development
Description

End-to-end formulation and process development services from early development through commercial scale-up, including excipient/API compatibility studies, pre-formulation work, and proof-of-concept prototypes designed with a Quality by Design (QbD) focus for pharmaceutical innovators, generics, and OTC companies.

2Analytical Services
CategoryAnalytical Testing
Description

Comprehensive analytical testing services including drug substance, drug product, and excipient testing, analytical method development and validation, QC release testing, and stability storage from -20C to 40C/75% RH for pharmaceutical customers.

3Clinical Manufacturing (CTM)
CategoryClinical Manufacturing
Description

cGMP clinical trial material manufacturing from 1 kg/liter to 50 kg/liter with brite stock packaging in bottles and blisters; supported 100+ clinical programs in the last 10 years for pharmaceutical innovators and small biotechs.

4Commercial Manufacturing
CategoryCommercial Manufacturing
Description

Over 40 years of commercial pharmaceutical manufacturing experience producing 400+ commercial SKUs across 100 product families annually, including integrated packaging, order fulfillment, distribution, and demand management services for pharmaceutical innovators and generics companies.

5Quality Services
CategoryQuality Assurance and Compliance
Description

Quality assurance and compliance services including rigorous supplier qualification, comprehensive analytical testing, cGMP-compliant processes with real-time monitoring, and continuous improvement culture supporting pharmaceutical customer regulatory requirements.

6Solid Dosage Form Manufacturing
CategorySolid Dosage Forms
Description

Manufacturing of tablets, capsules, powders, and granules with immediate and modified release capabilities, including wet high-shear/fluid bed granulation, dry granulation/compaction, and coating. Batch sizes from 0.5 to 1,000 kg. DEA Schedule II-V and OEB 3 capable.

7Semi-Solid Dosage Form Manufacturing
CategorySemi-Solid Dosage Forms
Description

Non-sterile creams, ointments, gels, lotions, and suppositories manufactured using vacuum deration and high-viscous polymer handling. Batch sizes from 3 to 1,000 kg. Located at the Mirabel, Quebec facility with 30+ years of experience.

8Oral Liquid Dosage Form Manufacturing
CategoryOral Liquid Dosage Forms
Description

Solutions, suspensions, and syrups manufactured using advanced mixing and homogenization with volume range from 10 to 4,400 liters, filled in plastic and glass bottles. DEA Schedule II-V capable, including pediatric specialties with taste-masking delivery systems.

9Sterile Injectable Manufacturing
Scale indicator9 records

Each record includes

Type, Value, Description, Source

Partnership1 partner
Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2026-04-14
Description

Apotex secured strategic sterile filling partnership with Halo Pharmaceuticals through an investment providing access to significant sterile injectable filling capacity at Halo's Whippany, New Jersey facility. The partnership supports Apotex's U.S.-based manufacturing strategy and sterile injectables network. The arrangement enables Apotex to access near-term sterile filling capacity as an alternative to greenfield development, providing operational flexibility. Apotex brings sterile processing experience, regulatory readiness expertise, and commercialization capabilities while securing access to vial and pre-filled syringe filling capacity. The partnership builds upon existing non-sterile manufacturing programs between the two companies.

Recent move8 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Cambrex is a leading North American small-molecule API and drug-product CDMO with a similar product portfolio to Halo. Most relevant peer — Halo was previously part of Cambrex (sold to Noramco Group in 2023), making this the closest historical and capability analog.

TypeDirect peer
Description

Metrics Contract Services is a US-based solid-dose and semi-solid CDMO focused on pharmaceutical innovators and generics. Directly comparable to Halo's solid dose and semi-solid business, with overlapping customer base and capabilities.

TypeDirect peer
Description

Curia (formerly AMRI) operates as a contract development and manufacturing organization offering API, drug product, and sterile fill-finish services. Directly comparable as a mid-sized integrated CDMO serving pharma innovators and generics with similar North American footprint.

TypeDirect peer
Description

Avara is a global CDMO providing solid dose, sterile, and API manufacturing services to large pharma. Directly comparable in dosage-form breadth and customer segments, particularly on the commercial manufacturing side.

TypeBroad incumbent
Description

PCI Pharma Services is a large integrated CDMO offering drug development, manufacturing, and packaging across multiple dosage forms including sterile injectables. Comparable to Halo's broad service offering but at meaningfully larger scale and global footprint.

TypeBroad incumbent
Description

Piramal Pharma Solutions is a global CDMO offering drug substance and drug product services including sterile fill-finish. Comparable to Halo in dosage-form breadth but with substantially larger global footprint and capacity.

TypeBroad incumbent
Description

Recipharm is a European-headquartered CDMO offering solid dose, semi-solid, sterile, and API services. Comparable to Halo in service categories, though operating primarily in Europe with broader geographic reach.

TypeBroad incumbent
Description

Aenova is a European CDMO providing solid dose, semi-solid, liquid, and sterile manufacturing services to pharma and consumer health companies. Comparable in dosage-form breadth to Halo though at larger scale and primarily European geography.

TypeBroad incumbent
Description

Siegfried is a global CDMO offering both API and drug product services including sterile fill-finish. Highly comparable — Siegfried acquired Halo's former parent Noramco Group's API assets in May 2026, making it both a peer and a recent counterparty in Halo's restructuring.

TypeBroad incumbent
Description

Thermo Fisher offers pharma services including drug product development, clinical manufacturing, and commercial supply across solid dose, sterile, and biologics. Overlaps with Halo across multiple service lines but at vastly larger scale and global footprint.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses4 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 highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers1 record

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 profile3 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

Feature5 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles3 records

Each record includes

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

No data
Compliance7 records

Each record includes

Name, Class, Description

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

Investors2 records

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 →

Halo Pharmaceutical

Pharmaceutical Contract Development and Manufacturing (CDMO)halopharma.com

Halo Pharmaceutical is a US-headquartered, Canada-manufactured contract development and manufacturing organization (CDMO) serving 85+ generic and branded pharmaceutical clients with solid dose, semi-solid, oral liquid, and sterile injectable products across 400+ commercial SKUs.

What Halo Pharmaceutical does

Halo Pharmaceutical is a contract development and manufacturing organization (CDMO) headquartered in Whippany, New Jersey, with primary manufacturing operations at a large-scale facility in Mirabel, Quebec, Canada. Founded in 2002 and historically part of the Noramco Group under SK Capital Partners ownership, the company emerged as a standalone CDMO in May 2026 following SK Capital's sale of Noramco to Siegfried. Halo Pharma provides development, manufacturing, and regulatory support services for solid oral dose, semi-solid, oral liquid, and sterile injectable pharmaceutical products, serving generic and branded pharmaceutical companies with a portfolio that includes 400+ commercial SKUs, 120 active development projects, and more than 90 ANDA/NDA filings to date.

The company's technical platform spans formulation development, analytical method development, validation, tech transfer, commercial manufacturing, and packaging across multiple dosage forms. The Mirabel site holds cGMP registrations with FDA, Health Canada, EMA, ANVISA, and MHRA, and operates under DEA registration for Schedule II-V controlled substances — a regulatory footprint that is uncommon among mid-tier CDMOs. The company has been actively expanding its technological capability, including a $30M+ investment in sterile injectable manufacturing anchored by a new Groninger ready-to-use vial filling line, and the addition of Gerteis dry granulation equipment for solid dose work.

Halo Pharma's business model is project-based contract services revenue: customers pay for development milestones, tech transfer, validation, and commercial manufacturing volumes under multi-year supply agreements. The customer base spans 85+ companies, including Top 10 pharmaceutical and generics players, with a strategic anchor relationship with Apotex covering sterile injectable capacity. Revenue is not publicly disclosed, but operational scale (Mirabel alone employs 200+ staff, with corporate headcount in the 101-250 range) and capital intensity are consistent with a mid-tier diversified CDMO serving both branded and generic pharmaceutical innovators.

Halo Pharmaceutical firmographics

Firmographics
Name
Halo Pharmaceutical
Legal name
Halo Pharma, Inc.
Website
https://halopharma.com
Company type
Private
Founded year
2002
Operating status
Operating
Headcount range
101–250 employees
Short description
Halo Pharmaceutical is a US-headquartered, Canada-manufactured contract development and manufacturing organization (CDMO) serving 85+ generic and branded pharmaceutical clients with solid dose, semi-solid, oral liquid, and sterile injectable products across 400+ commercial SKUs.
Ownership category
akta.pro rank

Halo Pharmaceutical industry classification

Industry
Product category
Pharmaceutical Contract Development and Manufacturing (CDMO)
NAICS
Pharmaceutical Preparation Manufacturing (325412), Pharmaceutical and Medicine Manufacturing (32541), Pharmaceutical and Medicine Manufacturing (3254)
SIC
Pharmaceutical Preparations (2834), Medicinal Chemicals & Botanical Products (2833)
akta.pro primary industry
Small-Molecule Drug Product (Solid/Oral/Parenteral) CDMO (HLAGABAB)
akta.pro secondary industries
Sterile Fill-Finish & Aseptic Manufacturing CDMO (HLAGABAH), Clinical Trial Material (CTM) Manufacturing & Supply CDMO (HLAGABAK)

Keywords

  • Pharmaceutical contract manufacturing
  • Drug product development
  • Contract development organization
  • Sterile injectable manufacturing
  • Pharmaceutical formulation services

Where Halo Pharmaceutical is headquartered

Location

Headquarters

HQ city
Whippany
HQ country
United States
HQ region
North America

Offices2 records

Markets served

Halo Pharmaceutical business model

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

Revenue model

  1. Contract Development and Manufacturing Services: Halo Pharma generates revenue through contract development and manufacturing services for pharmaceutical companies. Services include formulation development, analytical method development, clinical trial material manufacturing, commercial manufacturing, and tech transfer services. Revenue is generated through project-based contracts with pharmaceutical innovators, generics, and OTC companies for development and manufacturing services across solid dose, semi-solid, oral liquid, and sterile formats.

Pricing tiers

ModelBillingPrice
OtherMulti-year contractContract-based development and manufacturing services with custom project pricing

Go-to-market motion1 record

Distribution channels1 record

Marketing channels5 records

Halo Pharmaceutical product offering

Product offering

Core offering

Halo Pharma is a contract development and manufacturing organization (CDMO) that provides outsourced formulation development, analytical testing, clinical trial material manufacturing, and commercial-scale production of small molecule drug products. The company serves pharmaceutical innovators, generics manufacturers, and OTC product owners across solid dose, semi-solid, oral liquid, and (in 2026) sterile injectable dosage forms from two North American cGMP facilities in Whippany, NJ and Mirabel, Quebec.

Product overview

Halo Pharma is a contract development and manufacturing organization (CDMO) providing end-to-end pharmaceutical development and manufacturing services. The company operates two North American facilities in Whippany, NJ and Mirabel, Quebec, Canada. Core service modules include Development Services, Analytical Services, Clinical Manufacturing (CTM), Commercial Manufacturing, and Quality Services. These services support manufacturing across multiple dosage forms: Solid Dosage Forms (tablets, capsules, powders), Semi-Solid Dosage Forms (creams, ointments, gels), Oral Liquid Dosage Forms (solutions, suspensions, syrups), and Sterile Injectable Dosage Forms (vials, prefilled syringes, cartridges). The company is expanding into sterile manufacturing in 2026 with a $30+ million investment. An Accelerated Tech Transfer Program offers fixed-price engagements for GMP manufacturing in 16-20 weeks.

Differentiator

Problem solved

Functional benefit

Products and services

  • Development Services End-to-end formulation and process development services from early development through commercial scale-up, including excipient/API compatibility studies, pre-formulation work, and proof-of-concept prototypes designed with a Quality by Design (QbD) focus for pharmaceutical innovators, generics, and OTC companies.
  • Analytical Services Comprehensive analytical testing services including drug substance, drug product, and excipient testing, analytical method development and validation, QC release testing, and stability storage from -20C to 40C/75% RH for pharmaceutical customers.
  • Clinical Manufacturing (CTM) cGMP clinical trial material manufacturing from 1 kg/liter to 50 kg/liter with brite stock packaging in bottles and blisters; supported 100+ clinical programs in the last 10 years for pharmaceutical innovators and small biotechs.
  • Commercial Manufacturing Over 40 years of commercial pharmaceutical manufacturing experience producing 400+ commercial SKUs across 100 product families annually, including integrated packaging, order fulfillment, distribution, and demand management services for pharmaceutical innovators and generics companies.
  • Quality Services Quality assurance and compliance services including rigorous supplier qualification, comprehensive analytical testing, cGMP-compliant processes with real-time monitoring, and continuous improvement culture supporting pharmaceutical customer regulatory requirements.
  • Solid Dosage Form Manufacturing Manufacturing of tablets, capsules, powders, and granules with immediate and modified release capabilities, including wet high-shear/fluid bed granulation, dry granulation/compaction, and coating. Batch sizes from 0.5 to 1,000 kg. DEA Schedule II-V and OEB 3 capable.
  • Semi-Solid Dosage Form Manufacturing Non-sterile creams, ointments, gels, lotions, and suppositories manufactured using vacuum deration and high-viscous polymer handling. Batch sizes from 3 to 1,000 kg. Located at the Mirabel, Quebec facility with 30+ years of experience.
  • Oral Liquid Dosage Form Manufacturing Solutions, suspensions, and syrups manufactured using advanced mixing and homogenization with volume range from 10 to 4,400 liters, filled in plastic and glass bottles. DEA Schedule II-V capable, including pediatric specialties with taste-masking delivery systems.
  • Sterile Injectable Manufacturing

Quantifiable outcome

  • 120 active product development projects supported
  • +5 more outcomes

Companies that use Halo Pharmaceutical

Customer profile

Named customers1 record

Segments4 records

Ideal customer profiles3 records

Halo Pharmaceutical technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature5 records

Halo Pharmaceutical partnerships and signals

Strategic signal

Partnerships

One partnership is on record.

  • ApotexcoreStrategic or Co-development Partner · 14 April 2026Apotex secured strategic sterile filling partnership with Halo Pharmaceuticals through an investment providing access to significant sterile injectable filling capacity at Halo's Whippany, New Jersey facility. The partnership supports Apotex's U.S.-based manufacturing strategy and sterile injectables network. The arrangement enables Apotex to access near-term sterile filling capacity as an alternative to greenfield development, providing operational flexibility. Apotex brings sterile processing experience, regulatory readiness expertise, and commercialization capabilities while securing access to vial and pre-filled syringe filling capacity. The partnership builds upon existing non-sterile manufacturing programs between the two companies.

Scale indicators9 records

Recent moves8 records

Expansion highlights6 records

Halo Pharmaceutical competitors and assessment

Company assessment

Direct peers

  • Cambrex: Cambrex is a leading North American small-molecule API and drug-product CDMO with a similar product portfolio to Halo. Most relevant peer — Halo was previously part of Cambrex (sold to Noramco Group in 2023), making this the closest historical and capability analog.
  • Metrics Contract Services: Metrics Contract Services is a US-based solid-dose and semi-solid CDMO focused on pharmaceutical innovators and generics. Directly comparable to Halo's solid dose and semi-solid business, with overlapping customer base and capabilities.
  • AMRI (Curia): Curia (formerly AMRI) operates as a contract development and manufacturing organization offering API, drug product, and sterile fill-finish services. Directly comparable as a mid-sized integrated CDMO serving pharma innovators and generics with similar North American footprint.
  • Avara Pharmaceutical Services: Avara is a global CDMO providing solid dose, sterile, and API manufacturing services to large pharma. Directly comparable in dosage-form breadth and customer segments, particularly on the commercial manufacturing side.

Broad incumbents

  • PCI Pharma Services: PCI Pharma Services is a large integrated CDMO offering drug development, manufacturing, and packaging across multiple dosage forms including sterile injectables. Comparable to Halo's broad service offering but at meaningfully larger scale and global footprint.
  • Piramal Pharma Solutions: Piramal Pharma Solutions is a global CDMO offering drug substance and drug product services including sterile fill-finish. Comparable to Halo in dosage-form breadth but with substantially larger global footprint and capacity.
  • Recipharm: Recipharm is a European-headquartered CDMO offering solid dose, semi-solid, sterile, and API services. Comparable to Halo in service categories, though operating primarily in Europe with broader geographic reach.
  • Aenova Group: Aenova is a European CDMO providing solid dose, semi-solid, liquid, and sterile manufacturing services to pharma and consumer health companies. Comparable in dosage-form breadth to Halo though at larger scale and primarily European geography.
  • Siegfried Holding: Siegfried is a global CDMO offering both API and drug product services including sterile fill-finish. Highly comparable — Siegfried acquired Halo's former parent Noramco Group's API assets in May 2026, making it both a peer and a recent counterparty in Halo's restructuring.
  • Thermo Fisher Scientific (CDMO Services): Thermo Fisher offers pharma services including drug product development, clinical manufacturing, and commercial supply across solid dose, sterile, and biologics. Overlaps with Halo across multiple service lines but at vastly larger scale and global footprint.

Market position

Strengths5 records

Weaknesses4 records

Competitive moat5 records

Key risks6 records

Key highlights7 records

Customer concentration

Halo Pharmaceutical social profiles

Digital presence

Halo Pharmaceutical compliance and trust

Trust signal

Compliance7 records

Halo Pharmaceutical financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Halo Pharmaceutical leadership team

Management profile

Number of profiles

Profiles3 records

Halo Pharmaceutical funding detail

Funding detail

Funding overview

Funding rounds2 records

Investors2 records

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

Halo Pharmaceutical 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 Halo Pharmaceutical

What does Halo Pharmaceutical do?

Halo Pharma is a contract development and manufacturing organization (CDMO) that provides outsourced formulation development, analytical testing, clinical trial material manufacturing, and commercial-scale production of small molecule drug products. The company serves pharmaceutical innovators, generics manufacturers, and OTC product owners across solid dose, semi-solid, oral liquid, and (in 2026) sterile injectable dosage forms from two North American cGMP facilities in Whippany, NJ and Mirabel, Quebec.

Is Halo Pharmaceutical a public or private company?

Halo Pharmaceutical is a private company. It is classified as private equity controlled and is currently operating.

When was Halo Pharmaceutical founded?

Halo Pharmaceutical was founded in 2002. It employs 101 to 250 people.

Where is Halo Pharmaceutical based?

Halo Pharmaceutical is headquartered in Whippany, United States, in the North America region.

How does Halo Pharmaceutical make money?

One revenue line is on record: contract Development and Manufacturing Services.

Who are Halo Pharmaceutical's main competitors?

Direct peers on record are Cambrex, Metrics Contract Services, AMRI (Curia) and Avara Pharmaceutical Services. Broad incumbents are PCI Pharma Services, Piramal Pharma Solutions, Recipharm, Aenova Group, Siegfried Holding and Thermo Fisher Scientific (CDMO Services).

Does Halo Pharmaceutical have an API?

No public API is recorded for Halo Pharmaceutical.

What industry is Halo Pharmaceutical in?

Halo Pharmaceutical's product category is Pharmaceutical Contract Development and Manufacturing (CDMO). Its primary akta.pro industry code is HLAGABAB, Small-Molecule Drug Product (Solid/Oral/Parenteral) CDMO, with a secondary code of HLAGABAH, Sterile Fill-Finish & Aseptic Manufacturing CDMO. Its NAICS code is 325412 and its SIC code is 2834.

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Live signals
PharmTechQ&A: Sterile Injectable Manufacturers Gain New CDMO Option as Halo ExpandsHalo Pharma is finalizing the construction and startup of a new sterile fill-finish manufacturing platform designed to support sterile injectable production from clinical development through commercial supply. The facility utilizes Groninger filling technology and SKAN isolator systems, with site acceptance testing scheduled before media fills begin toward the end of 2026. This expansion provides sponsors with flexible container formats including prefilled syringes, vials, and cartridges.PharmTechQ&A: Why Is Halo Pharma Expanding Into Sterile Injectables Now?Halo Pharma is launching a new sterile fill-finish manufacturing platform to produce syringes, vials, and cartridges, aiming to meet growing domestic demand for US-based injectable production. The company secured Apotex as an anchor customer to facilitate early FDA inspections and has divested its API business to focus on drug product manufacturing. This expansion positions Halo as the only US manufacturer capable of producing oral solids, liquids, injectables, and blow-fill-seal products within a single network.NewswireApotex Announces First Quarter 2027 ResultsApotex reported Q1 FY2027 results with Canada revenue up 11% to $413 million, while U.S. revenue excluding VLLP fell 9%. Adjusted EBITDA was $259 million, a 31% margin, and the company applied $800 million of IPO proceeds to debt repayment. It guided to upper mid-single-digit revenue growth and ~30% adjusted EBITDA margin for FY2027.SpecchemonlineSK Capital completes two exitsPrivate investment firm SK Capital Partners has completed two previously announced portfolio company sales: Noramco, Extractas Biosciences, and Purisys were sold to Siegfried, while Phoenix Flavors & Fragrances was sold to Turpaz Industries, with terms undisclosed. SK Capital is retaining Halo Pharmaceuticals, which operates sterile-fill-finish facilities in the US and controlled substance production in Canada, with a sterile injectable manufacturing facility expected online in the second half. Turpaz Industries, which already owns a portfolio of flavors and fragrances companies in North America, stated that Phoenix represents a strong strategic fit for its organization.PharmiWeb.comPharmiWeb.com – Thank youPharmiWeb.com is closing after 28 years, having operated since 1998. The company thanks members, advertisers, partners, and readers for their contributions. It notes the site was among the first in the dot-com era.PR NewswireApotex Announces Strategic U.S. Sterile Filling Partnership with Halo PharmaceuticalsApotex Corp. announced a strategic sterile filling partnership with Halo Pharmaceuticals on April 14, 2026, providing Apotex access to a significant portion of sterile injectable filling capacity being installed at Halo's Whippany, New Jersey facility. The investment supports Apotex's U.S.-based manufacturing strategy and sterile injectables network while offering operational flexibility as an alternative to greenfield development. The partnership builds on existing non-sterile manufacturing programs between the two companies and includes vial and pre-filled syringe filling capabilities.GlobeNewswireHalo Pharma Enhances Manufacturing Capabilities with Macro-Pactor® InvestmentHalo Pharma, a contract development and manufacturing organization (CDMO), announced the addition of a Gerteis Macro-Pactor® roller compactor at its Whippany, New Jersey facility, with the equipment expected to be operational in Q1 2026. The investment enables seamless scale-up from early-phase development using Halo's existing Mini-Pactor® to late-stage commercial production, enhancing dry-granulation capabilities for complex formulations including moisture-sensitive APIs and high-drug-load products. The company stated the equipment reduces scale-up risk, timelines, and reformulation needs while improving operator safety through its closed, dust-contained design.GlobeNewswireKane Biotech Makes First Commercial Sale of revyve™ Antimicrobial Wound Gel to ProgenaCare GlobalKane Biotech made its first commercial sale of revyve Antimicrobial Wound Gel to ProgenaCare Global, fulfilling its obligation on the $500,000 initial manufacturing scale-up fee. The product received FDA 510(k) clearance, and Kane signed a four-year manufacturing agreement with Halo Pharma for production in Quebec.GlobeNewswireCambrex Completes Acquisition of Halo PharmaCambrex completed its acquisition of Halo Pharma for approximately $425 million, adding formulation development and finished dosage manufacturing capabilities. The deal expands Cambrex's global API network with two North American facilities, and the combined business creates a leading small molecule CDMO with both API and finished dosage capabilities.GlobeNewswireCambrex Reports Second Quarter 2018 Financial ResultsCambrex reported Q2 2018 net revenue of $152.0 million, up 13% year-over-year, and diluted EPS of $1.21. The company reaffirmed its full-year adjusted net revenue growth and EBITDA guidance, and agreed to acquire Halo Pharma for about $425 million in cash.