Listed Pharmaceuticals Companies in Iowa

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

Apotheca

📍 Woodbine, IA Est. 1987
Specialties: Homeopathic ManufacturingHerbal ProductsOTC PharmaceuticalsNutritional Supplements

Apotheca is an FDA-registered, third-party certified manufacturing facility with over 30 years of experience in the production of over-the-counter (OT...

Grato Holdings

📍 Woodbine, IA Est. 2011
Specialties: Homeopathic RemediesHerbal ExtractsDietary SupplementsMedicinal Chemicals

Grato Holdings is a distinguished pharmaceutical manufacturing company established in 2011, serving as the parent company for Apotheca Inc., Energique...

JRS Pharma

📍 Cedar Rapids, IA Est. 1990
Specialties: Pharmaceutical ExcipientsBindersDisintegrantsLubricants

JRS Pharma is a leading manufacturer of pharmaceutical excipients offering a complete portfolio of solutions for the global health science industry. A...

Katecho

📍 Des Moines, IA Est. 1984
Specialties: Medical Contract ManufacturingHydrogel ManufacturingDisposable Therapy ElectrodesPatient Monitoring Systems

Katecho, LLC is a specialized medical contract manufacturer based in Des Moines, Iowa, dedicated to advancing pharmaceutical and medical device innova...

Maharishi Ayurveda Products International

📍 Fairfield, IA Est. 1985
Specialties: Ayurvedic ProductsHerbal ManufacturingNatural Skin CareMassage Oils

Maharishi Ayurveda Products International is the first and oldest ayurveda products company in the United States, founded in 1985 with 39 years of ope...

Surmasis Pharmaceutical

📍 Des Moines, IA Est. 2010
Specialties: Transdermal Patch ManufacturingHydrogel Reservoir PatchesMatrix/Solvent PatchesFDA Clinical Batches

Surmasis is a contract pharmaceutical manufacturer with a passion for bringing ideas to life, specializing in transdermal patch manufacturing. The com...

Iowa pharmaceuticals manufacturer landscape

Compare listed pharmaceuticals manufacturer profiles in Iowa 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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