Aarise Pharma is a WHO-GMP certified manufacturer and exporter of Active Pharmaceutical Ingredients (APIs), based in Haridwar, India. We supply bulk APIs across multiple therapeutic categories to generic drug manufacturers, contract formulators, and pharmaceutical distributors worldwide.

What Are Active Pharmaceutical Ingredients?

An Active Pharmaceutical Ingredient (API) is the component of a drug that produces its intended therapeutic effect. APIs are manufactured to strict pharmacopoeial standards (USP/BP/EP) and combined with excipients during formulation to create the final dosage form.

API Categories We Manufacture

Steroid APIs

Testosterone, corticosteroids, anabolic steroids, prednisolone, dexamethasone, and related compounds, manufactured under cGMP conditions with full analytical characterization.

Peptide APIs

Semaglutide, insulin analogs, oxytocin, GLP-1 agonists, and other peptide APIs, available in lyophilized and solution form.

Hormone APIs

Testosterone cypionate, HGH, levothyroxine, estradiol, progesterone, and related hormone raw materials.

General Pharmaceutical APIs

Metformin, atorvastatin, amoxicillin, omeprazole, losartan, and other widely used generic APIs across therapeutic categories.

Quality Documentation & Certifications

Our Haridwar facility is WHO-GMP certified and ISO 9001:2015 certified. Every shipment includes a Certificate of Analysis (COA) and Material Safety Data Sheet (MSDS), with Certificate of Pharmaceutical Product (CPP), Drug Master File (DMF), and Certificate of Suitability (CEP) documentation available on request.

Beyond Bulk APIs

Aarise Pharma also manufactures dispersible tablet formulations and offers third-party contract manufacturing for finished dosage forms.

Where We Export

See our full list of API export markets, with dedicated supplier guides covering regulatory requirements and shipping logistics for each country.

Frequently Asked Questions

What is an Active Pharmaceutical Ingredient (API)?

An Active Pharmaceutical Ingredient (API) is the biologically active component of a drug product responsible for its therapeutic effect. APIs are combined with excipients during formulation to produce the final dosage form — tablets, capsules, injectables, or dispersible tablets.

What certifications does Aarise Pharma hold?

Aarise Pharma’s Haridwar facility is WHO-GMP certified and ISO 9001:2015 certified. Certificate of Pharmaceutical Product (CPP), Drug Master File (DMF) references, and Certificate of Suitability (CEP) documentation are available on request for markets that require them.

What documentation is included with every API shipment?

Every shipment includes a Certificate of Analysis (COA) with batch-specific test results and a Material Safety Data Sheet (MSDS). HPLC chromatograms and impurity profiles are available on request.

Which countries does Aarise Pharma export APIs to?

Aarise Pharma currently exports to 18+ countries across Latin America, North America, Europe, and Asia, with dedicated supplier guides covering local regulatory requirements for each market.

Does Aarise Pharma offer third-party manufacturing in addition to bulk API supply?

Yes. In addition to bulk API export, Aarise Pharma’s Haridwar facility offers third-party contract manufacturing for dispersible tablets and other finished dosage forms.

Ready to order? Contact Aarise Pharma for API pricing, specifications, and samples.