GMP-approved API manufacturing in Bharuch, Gujarat  ·  Talk to our pharma experts →

Pure APIs.
Trusted manufacturing,
backed by 43 years of business excellence.

We manufacture Active Pharmaceutical Ingredients and pharma-grade solvents at our cGMP-compliant facility in Bharuch, Gujarat — under loan licensing, with manufacturing licenses already in place. Free samples. Full regulatory support.

cGMP-compliant Licensed manufacturing Free samples NDA upfront
43+
Years of group heritage
100%
cGMP-compliant facility
10+
Licensed APIs & solvents
18+
Reaction capabilities

From qualification to dispatch — in 4 clear steps.

A confidential, structured engagement designed for pharma procurement, regulatory affairs, and quality teams.

STEP 01
Share your requirement

Tell us your API or solvent of interest, grade (IP / USP / BP / EP), pharmacopoeial requirement, and indicative volumes. NDA signed upfront.

STEP 02
Free sample & qualification

We submit samples free of cost for your evaluation and source qualification. Full COA and documentation provided.

STEP 03
Agreement & scheduling

We formalise commercial terms, regulatory commitments, and production schedules — regular or campaign-basis as required.

STEP 04
Manufacture & dispatch

Production runs at our cGMP-compliant Bharuch facility. Full traceability and pharmacopoeial compliance on every batch.

What we do for pharma companies.

Pon Pure Chemical India Pvt. Ltd. is one of the reputed and highly diversified companies in the field of Active Pharmaceutical Ingredients and solvents for the pharmaceutical industry.

Our API manufacturing operations run at our cGMP-compliant loan-licensing site in Bharuch, Gujarat. We hold valid manufacturing licenses for a focused portfolio of APIs and pharma-grade solvents — produced on regular and campaign basis.

Promoted by a well-known Indian business house with 43+ years of heritage, founded in 1981 by our Chairman & MD Mr. Ponnuswami, we deliver effective solutions that protect both your business and the environment.

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cGMP-compliant facility

Manufacturing at a cGMP-compliant loan-licensing site in Bharuch, Gujarat — built for regulated-market supply.

ICH Q7 & manufacturing licenses

Production runs under ICH Q7 guidelines for APIs & intermediates — manufacturing licenses already in hand.

Free samples for qualification

We submit samples at no cost to support your source qualification and stability studies.

Regular & campaign basis production

Highlighted APIs are produced on a regular basis; others are scheduled on campaign basis to suit your demand.

Built for pharmaceutical innovators.

If your business needs reliable API supply, pharma-grade solvents, or a qualified secondary source — we can support.

Formulation Companies

API supply for tablets, capsules, syrups, and topical formulations across regulated and semi-regulated markets.

Regular supply
Pharma Solvent Buyers

Pharmacopoeial-grade solvents (IP / BP / USP / EP) for use as reaction media, purification, and finished-dosage manufacturing.

License available
Contract Manufacturers

Reliable secondary or campaign-basis source for niche APIs where production flexibility and traceability matter.

Campaign basis
Don't see your molecule?

If your requirement is outside our current licensed portfolio, talk to us — we'll assess fit and capacity transparently.

Tell us your requirement →

India's trusted manufacturer of Pharma APIs.

Active Pharmaceutical Ingredients across human health and veterinary categories — manufactured under valid licenses, ICH Q7-compliant, with COA and DMF support available on request.

Sr. No Product Name Pharmacopoeia Drug Category Therapeutic Use Manufacturing Action
01 Minoxidil IP USP BP Human Anti-Hypertensive / Hair Growth Regular Send Enquiry
02 Propranolol HCl IP USP BP Human Anti-Hypertensive Regular Send Enquiry
03 Etoricoxib IP IH Human Anti-Inflammatory Regular Send Enquiry
04 Montelukast Sodium USP Human Leukotriene Receptor Antagonist (LTRA) Campaign Send Enquiry
05 Carvedilol USP Human Anti-Hypertensive Campaign Send Enquiry
06 Dextromethorphan HBr USP Human Anti-Tussive Campaign Send Enquiry
07 Albendazole IP BP USP Human / Vet Anthelmintic Regular Send Enquiry
Sr. No Product Name Pharmacopoeia Drug Category Therapeutic Use Manufacturing Action
01 Albendazole IP BP USP Human / Vet Anthelmintic (Veterinary) Regular Send Enquiry
Looking for additional veterinary APIs? Talk to us — we evaluate veterinary requirements case-by-case based on volume, regulatory market, and licensing fit.
Sr. No Product Name Pharmacopoeia Drug Category Use Manufacturing Action
01 Iso Propyl Alcohol (IPA) IP BP USP Solvent Pharma Solvent Licensed Send Enquiry
02 Propylene Glycol IP BP Excipient Excipient / Solvent Licensed Send Enquiry
03 Dichloromethane USP BP EP Solvent Reaction Solvent Licensed Send Enquiry
04 Acetone IP BP USP Solvent Pharma Solvent Licensed Send Enquiry
05 Glycerin IP BP USP Excipient Excipient / Humectant Licensed Send Enquiry
06 Monoethanolamine USP-NF Excipient Excipient (USP System) Licensed Send Enquiry
07 Triacetin USP BP Excipient Excipient / Solvent Licensed Send Enquiry
08 Glycerol Formal IH Solvent Veterinary Solvent Licensed Send Enquiry
All solvents listed above are manufactured under valid licenses. Pharmacopoeial-grade output (IP / BP / USP / EP) with batch-level COA. Custom packaging and bulk supply available.
Sr. No Product Name Pharmacopoeia Drug Category Use Status Action
01 Light Liquid Paraffin IP BP USP Excipient Excipient / Lubricant In Development Express Interest
02 Petroleum Jelly IP BP USP Excipient Topical Base / Emollient In Development Express Interest
03 PEG 6000 (Polyethylene Glycol 6000) IP BP USP Excipient Excipient / Solid Dosage Binder In Development Express Interest
Products under development: Our R&D and pilot-plant teams are actively working on these molecules for our licensed portfolio. Express interest below to be notified when commercial supply becomes available.
Documentation available: Specifications, Method of Analysis, COA, Stability data, Process flow charts, and DMF support — provided on request under signed NDA. CAS numbers and detailed technical packages shared during qualification.

Reaction chemistry & facility infrastructure.

Eighteen reaction types and a full set of pharma-grade infrastructure capabilities — supporting both regular production and contract / campaign manufacturing under NDA.

Reaction Capabilities
Aromatic Bromination
Esterification
Aliphatic Bromination
Condensation Reaction
Chlorination
Mannich Reaction
Hydrogenation
Grignard Reaction
Nitration
Friedel-Craft Reaction
Oxidation
Sandmeyer Reaction
Reduction
Suzuki Reaction
Diazotization
Ullmann Coupling
Methoxylation
Reduction Reaction
Facility & Compliance
  • cGMP-compliant manufacturing facilities
  • Contract Research & Contract Manufacturing under NDA / CDA
  • GMP solid API production in Class 8
  • High-Pressure Reactions up to 20 kg/cm²
  • High Temperature up to 240°C
  • High Vacuum Distillation up to 0.02 Torr
  • Hazardous Chemical Reactions — Li, BH₄, Synhydride
  • Pilot-Plant facility for new molecule scale-up & development
  • Precious Catalyst Reactions — Pt, Pd, Rh
  • Production under ICH Q7 guidelines for APIs & Intermediates
  • Well-designed equipment for Effluent handling, MEE & ETP

R&D for pharma applications.

With a team strength of over 45 professionals, including doctorates and postgraduates in specialised disciplines, we continue to grow with a vision to become the most preferred global chemical partner — delivering high-quality products, innovative solutions, and exceptional service.

We embrace eco-friendly and sustainable practices that deliver long-term value to both industry and the environment, while maintaining rigorous quality control at every stage to ensure consistency, reliability, and excellence in every product. By harnessing advanced technology and innovative thinking, we develop high-performance, next-generation chemical solutions.

HPLC
High-Performance Liquid Chromatography
GC
Gas Chromatography
FTIR
Fourier-Transform Infrared Spectroscopy
Discuss your R&D needs
R&D Laboratory
45+
Specialised researchers
Doctorates & postgraduates

More from Pon Pure Chemicals.

Our pharma division is one part of a larger chemicals ecosystem. Explore the other divisions of Pon Pure Chemicals Group.

Trusted across industries & borders.

Decades of proven excellence in chemical manufacturing, distribution, and supply chain — built on quality, compliance, and customer-specific solutions.

  • 1
    44+ Years of Chemical Leadership
  • 2
    Global Sourcing + Massive Storage = Zero Stockouts
  • 3
    Specialty Chemical Manufacturing Across Key Segments
  • 4
    Zero-Rejection Repacking & Nationwide Facilities
  • 5
    GPS-Tracked Logistics & End-to-End Supply Chain Control
  • 6
    Advanced R&D, QA/QC Labs & Technical Application Support
  • 7
    Serving 60+ Industries, 65+ Countries & 13,000+ Customers

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All details are kept strictly confidential under NDA.

Your data is never shared. NDA offered on first call.