Divine Laboratories


Manufacturer of finished pharmaceutical formulations since 1994. Operates WHO‑GMP / cGMP manufacturing facilities supporting multiple dosage forms including sterile parenteral injectables, oral solids, topical semisolids, ophthalmic solutions, ENT/nasal drops and veterinary injectables. Offers contract/third‑party and loan‑license manufacturing, formulation development and scale‑up, in‑house analytical and microbiological testing, and regulatory dossier support for domestic and export markets.

Industries

manufacturing
pharmaceutical
wholesale

Nr. of Employees

medium (51-250)

Divine Laboratories

24/B, Sahajanand Industrial Estate, Mujmahuda, Vadodara - 390020, Gujarat, India


Products

Sterile parenteral injectables (human and veterinary)

Sterile injectable formulations produced and packaged as vials, ampoules or prefilled syringes across therapeutic categories including antibiotics, anesthesia agents, anticoagulants, vasopressors and nutritional injectables.

Ophthalmic solutions and eye drops

Sterile ophthalmic solutions and eye drops manufactured and packaged for clinical ophthalmic use.

ENT and nasal drops / ear drops

Liquid formulations for ENT and nasal administration and ear drops produced in primary dropper assemblies.

Topical creams, ointments and gels

Semisolid topical formulations manufactured and packaged in tubes and ointment containers for dermatological and antiseptic use.

Dental care: medicated toothpaste gel

Manufacture of dental care paste/gel formulations for retail dental hygiene use.

Vitamin and nutritional injections; oral vitamin products

Parenteral vitamin preparations and oral vitamin capsule offerings produced for clinical and retail supply.


Services

On‑site manufacture of finished pharmaceutical formulations under contract for domestic and export markets, including third‑party packaging, labeling and export documentation support.

On‑site R&D and formulation development with capability to convert formulations into development, pilot and production batches across sterile and non‑sterile dosage forms.

On‑site chemical and microbiological testing for raw materials and finished products, including sterility, endotoxin and chromatographic assays for batch release.

Regulatory support including preparation of technical documentation up to CTD format for market submissions and export registrations.

Expertise Areas

  • Sterile parenteral manufacturing
  • Formulation development and scale‑up (sterile and non‑sterile)
  • Lyophilization and lyophilized product handling
  • Oral solid dose and semisolid manufacturing
  • Show More (7)

Key Technologies

  • Aseptic vial, ampoule and prefilled syringe filling
  • Lyophilization (freeze‑drying)
  • Sterile filtration and sterilization processes
  • Tablet compression and capsule filling
  • Show More (6)

News & Updates

Award for outstanding exports performance by the Pharmaceuticals Export Promotion Council of India for 2016-17.

Recognized as a fastest growing pharmaceutical SME in exports by Pharma Excellence Award Council, India for 2016-17.

Recognized by Pharma Excellence Awards Council, India for export performance during 2015-2016.


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