Listed Pharmaceuticals Companies in Rhode Island

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

Denison Pharmaceuticals

📍 Lincoln, RI Est. 1980
Specialties: Liquids, creams, lotions, gels, and ointmentsShort to medium-run product manufacturingCustom formulation developmentCommercial batch sizes up to 2,000 gallons

A specialized pharmaceutical contract manufacturing and packaging services company with over four decades of experience. Denison focuses on formulatin...

Rhodes Pharmaceuticals LP

📍 Coventry, RI Est. 2008
Specialties: Generic pharmaceutical productsSpecialty pharmaceutical developmentProduct distribution servicesQuality pharmaceutical formulations

A subsidiary of Purdue Pharma L.P., Rhodes Pharmaceuticals has developed and distributed quality pharmaceutical products nationwide since 2008. The co...

Tedor Pharma Services Inc

📍 Cumberland, RI Est. 2005
Specialties: Solid dosage forms (tablets, capsules)DEA-scheduled productsHigh potency compoundsPowder biologics

A science-driven Contract Development and Manufacturing Organization specializing in solid dosage pharmaceutical development and manufacturing. Tedor ...

Wexford Laboratories Inc

📍 Warwick, RI Est. 1985
Specialties: Tablets and capsulesCreams and topical preparationsInjectable productsSuspensions and syrups

An established pharmaceutical manufacturer with over 35 years of industry experience, developing and manufacturing nearly 200 high-quality medicines. ...

Rhode Island pharmaceuticals manufacturer landscape

Compare listed pharmaceuticals manufacturer profiles in Rhode Island 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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