Listed Pharmaceuticals Companies in Oklahoma

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

ARL Bio Pharma

📍 Oklahoma City, OK Est. 1998
Specialties: HPLC TestingHPLC-MS/MS TestingGas ChromatographyMicrobiological Testing

Contract testing laboratory providing analytical and microbiological testing for pharmaceutical manufacturers, compounding pharmacies, and dietary sup...

Biolytx Pharmaceuticals

📍 Oklahoma City, OK Est. 2005
Specialties: Antimicrobial PeptidesCAP37 Protein-Based TherapeuticsWound Healing CompoundsAnti-Infective Drugs

Biolytx Pharmaceuticals is an emerging drug development company based in Oklahoma City, Oklahoma, dedicated to confronting the critical challenge of a...

Charlesson LLC

📍 Oklahoma City, OK Est. 2003
Specialties: Ocular TherapeuticsMacular Degeneration TreatmentsDiabetic Retinopathy DrugsSmall Molecule Therapeutics

Charlesson LLC operates as a specialized pharmaceutical contract research organization based in Oklahoma City, Oklahoma, focusing on advanced ocular t...

Cytovance Biologics

📍 Oklahoma City, OK Est. 2003
Specialties: Therapeutic ProteinsAntibodiesMammalian Cell CultureMicrobial Fermentation

Biopharmaceutical contract development and manufacturing organization specializing in therapeutic proteins and antibodies from mammalian cell culture ...

Tetherex Pharmaceuticals

📍 Oklahoma City, OK
Specialties: Selectin InhibitionAnti-Inflammatory TherapeuticsCOPD TreatmentsAsthma Treatments

Clinical-stage biopharmaceutical company developing therapeutics for inflammation and tumors across severe diseases....

Oklahoma pharmaceuticals manufacturer landscape

Compare listed pharmaceuticals manufacturer profiles in Oklahoma 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.

Need Help Finding Pharmaceuticals in Oklahoma?

Our directory makes it easy to research listed manufacturing companies.