Listed Pharmaceuticals Companies in Minnesota

Results are ordered alphabetically. Inclusion is based on the matching process or industry recorded on each published profile.

ANI Pharmaceuticals, Inc.

📍 Baudette, MN Est. 2003
Specialties: Branded Prescription PharmaceuticalsGeneric PharmaceuticalsSpecialty Pharmaceutical Development

ANI Pharmaceuticals, Inc. is a leading specialty pharmaceutical manufacturer based in Baudette, Minnesota, dedicated to developing, manufacturing, and...

AVEKA Group

📍 Woodbury, MN Est. 1994
Specialties: Custom Pharmaceutical FormulationsAPI ProcessingSpray DryingParticle Encapsulation

Contract manufacturing and R&D company since 1994 specializing in fine particle production and pharmaceutical processing services with 30+ years of ex...

Bell Pharmaceuticals Inc.

📍 Belle Plaine, MN Est. 2001
Specialties: OTC PharmaceuticalsPharmaceutical PackagingCaffeine SupplementsSleep Aids

Bell Pharmaceuticals Inc. stands as a dedicated pharmaceutical manufacturing company founded in 2001 and strategically located in Belle Plaine, Minnes...

Paddock Laboratories, LLC

📍 Minneapolis, MN
Specialties: Generic Prescription PharmaceuticalsOTC Specialty ProductsPharmaceutical Manufacturing

Established pharmaceutical manufacturer specializing in generic prescription medications and over-the-counter specialty products with extensive manufa...

Tapemark

📍 West St. Paul, MN
Specialties: Transdermal Drug Delivery SystemsOral Thin FilmsUnit Dose Semi-Solid FormulationsCDMO Services

Full-service Contract Development and Manufacturing Organization specializing in unit dose semi-solid drug delivery systems with state-of-the-art manu...

Upsher-Smith Laboratories, LLC

📍 Maple Grove, MN Est. 1919
Specialties: Brand MedicationsGeneric PharmaceuticalsContract ManufacturingOral Solid Dosage Manufacturing

Trusted U.S. pharmaceutical company since 1919 with new $100M, 270,000 sq ft manufacturing facility. Specializes in brand medications for migraine and...

Minnesota pharmaceuticals manufacturer landscape

Compare listed pharmaceuticals manufacturer profiles in Minnesota by process fit, location, and the documentation the buyer can actually verify.

Clusters this page covers

  • New Jersey and Pennsylvania finished-dose, packaging, and pharmaceutical-chemical corridor
  • North Carolina research-triangle and sterile or biologic-adjacent manufacturing
  • Illinois and Massachusetts specialty, sterile, and research-adjacent production
  • California clinical, specialty, and West Coast packaging and distribution nodes

Selection rules

  1. Match dosage form first: solid oral, liquid, sterile, topical, or packaging-only. A listed pharmaceutical plant is not automatically qualified for every form.
  2. Confirm FDA registration, license, and the last inspection or quality-system evidence the company will share.
  3. Ask which operations stay on site versus get contracted, including testing, serialization, and packaging.
  4. Require the same batch size, release-test panel, and change-control rules from every shortlisted site.
  5. Separate clinical or development capacity from commercial supply. Those are different operating models.
  6. Use state pages when the program needs on-site audits, controlled-substance proximity, or a regional packaging node.

When to use a finished-dose plant, a packager, or a development site

A pharmaceutical manufacturer can be a commercial plant, a packager, or a development lab. Choose the site type before comparing listed profiles.

When this is the jobUseWhy
Commercial finished-dose supply with batch records and release testingcGMP finished-dose manufacturerThe award depends on registered process, documentation, and inspection history.
Primary or secondary packaging, serialization, or labeling onlyPharmaceutical packagerThe product is already made; the constraint is coding, artwork, and distribution-ready pack-out.
Clinical, scale-up, or formulation development before commercial transferDevelopment or CDMO siteThe buyer needs process development and tech-transfer evidence, not only commercial volume.

How to source this work

Use a pharmaceutical manufacturer when cGMP, FDA registration, dosage form, contamination control, and batch documentation—not general contract manufacturing capacity—are the buying criteria.

Include in the RFQ

  • dosage form, batch size, and commercial or clinical intent
  • required registrations, licenses, and quality-system scope
  • raw-material, packaging-component, and approved-source rules
  • in-process, release, and stability testing requirements
  • serialization, labeling, storage, and change-control expectations

Questions that separate suppliers

  • Is the site registered and inspected for this dosage form?
  • Which operations are performed in-house versus by a qualified contractor?
  • What batch records, COAs, and deviation history will the buyer receive?

Questions this page can answer

How should a buyer compare pharmaceutical manufacturers?

Start with dosage form, registration, and quality-system scope. Then compare which operations are on site, what batch records look like, and whether the site is set up for clinical or commercial supply. Directory listing is not an FDA approval.

Which states should pharmaceutical buyers check first?

New Jersey, Pennsylvania, North Carolina, Illinois, and Massachusetts are the first UNITEMFG state-and-category pages to open. California remains important for specialty, clinical, and West Coast packaging work.

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