Listed Pharmaceuticals Companies in Mississippi

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

Edwards Pharmaceuticals

📍 Ripley, MS Est. 1988
Specialties: Urology ProductsGastroenterologyOncologyWound Care

Pharmaceutical manufacturer specializing in multiple therapeutic areas including Urology, Gastroenterology, Antihistamine, Decongestant, Expectorant p...

GCP Laboratories Mississippi

📍 Gulfport, MS Est. 2010
Specialties: Liquid AntacidsOver-the-Counter MedicationsMagnesium Hydroxide API

World's leading manufacturer of liquid antacids and over-the-counter liquid medications. Specializes in magnesium hydroxide API production and powder ...

Misemer Pharmaceutical

📍 Ripley, MS Est. 1948
Specialties: Innovative Prescription ProductsTherapeutic Pharmaceuticals

Specialty pharmaceutical company commercializing innovative prescription products with 75+ years in business. Focus on innovative prescription product...

Natureplex

📍 Olive Branch, MS Est. 2000
Specialties: Over-the-Counter PharmaceuticalsPersonal Care ProductsPrivate Label Manufacturing

Natureplex operates as a leading pharmaceutical manufacturer based in Olive Branch, Mississippi, specializing in high-quality healthcare products and ...

WraSer Pharmaceuticals

📍 Ridgeland, MS Est. 2000
Specialties: Specialty Pharmaceutical ProductsProprietary Pharmaceutical Development

Independent specialty pharmaceutical marketing and distribution company focusing on specialty pharmaceutical products and proprietary pharmaceutical d...

Mississippi pharmaceuticals manufacturer landscape

Compare listed pharmaceuticals manufacturer profiles in Mississippi 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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