Pharmaceutical &
Veterinary APIs
Manufactured in India & Germany
Afro Pharmacy delivers superior-grade Active Pharmaceutical Ingredients to global pharmaceutical and veterinary companies. Dual-certified manufacturing sites. Uncompromising quality. Reliable supply since 2021.
Our API Products
Advancing Global Healthcare Through API Excellence
Since 2021, Afro Pharmacy has been manufacturing and supplying high-purity Active Pharmaceutical Ingredients from our dual facilities in India and Germany. We serve pharmaceutical formulators, veterinary drug companies, research institutions, and contract manufacturers across 30+ countries worldwide.
Purity across all API product lines
Your Reliable API Manufacturing Partner
We combine the manufacturing efficiency of our India facility with the European regulatory precision of our Germany site — giving our global clients the best of both worlds in a single, trusted supply relationship.
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Research-Grade to Commercial Scale We supply APIs from milligram reference quantities to multi-kilogram commercial batches, scaling with your development pipeline.
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Full Regulatory Documentation CoA, SDS, DMF support, stability data, and method validation packages — everything needed for your regulatory submissions.
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Contract Manufacturing Available Long-term CMO agreements, custom API synthesis, and intermediate manufacturing tailored to client specifications.
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Dual-Continent Supply Security Two independent manufacturing sites ensure uninterrupted supply continuity and multi-regional regulatory compliance.
Active Pharmaceutical Ingredients
Pharmaceutical and veterinary-grade APIs manufactured under strict GMP conditions. Each product is fully documented and available for global export.
A short-acting imidazole-based IV anaesthetic agent widely used for induction of general anaesthesia and sedation of critically ill patients. Produced under WHO-GMP conditions at our India and Germany facilities.
An imidazole-based non-barbiturate sedative and immersion anaesthetic for aquaculture and veterinary use. Also functions as Etomidate EP Impurity B for pharmaceutical reference standards.
A dissociative anaesthetic and NMDA receptor antagonist structurally related to ketamine. Used in veterinary medicine for immobilisation of wild and domestic animals, typically combined with zolazepam.
Built on Quality.
Delivered with Reliability.
From synthesis to documentation to delivery — every step is engineered to meet the expectations of the world’s most demanding pharmaceutical markets.
Rigorous Analytical QC
Every batch undergoes multi-stage testing — HPLC assay, related substances, residual solvents, heavy metals, and microbial limits — with full CoA documentation issued before release.
Multi-Regulatory Compliance
Our products meet USP, BP, and EP pharmacopoeia standards. Our Germany facility holds EU GMP status; our India facility is WHO-GMP certified — enabling global market access.
Dual-Site Manufacturing
Two independent facilities across two continents eliminate single points of failure and provide supply resilience that pharmaceutical clients can rely on for uninterrupted production.
Complete Documentation
DMF support, SDS, CoA, stability study reports, impurity profiles, and method validation packages — everything your regulatory team needs in one place.
Scale-Ready Supply
From milligram reference standards for R&D to multi-kilogram commercial batches — we scale with your pipeline, with consistent quality at every quantity.
Long-Term CMO Partnerships
We build sustained relationships through contract manufacturing agreements, custom synthesis, and dedicated account management — not one-off transactions.
Two Countries. One Standard of Excellence.
Our strategically positioned manufacturing sites in India and Germany give Afro Pharmacy a unique dual-continent advantage — combining Asian production efficiency with European regulatory standards.
India Facility
Primary Manufacturing HubOur India facility is our flagship production site, equipped with state-of-the-art synthesis infrastructure, in-house analytical laboratories, and a fully documented WHO-GMP quality management system. It serves as the backbone of our API supply to Asian, African, and Middle Eastern markets.
- WHO-GMP Certified Manufacturing
- In-house HPLC & multi-parameter analytical QC
- USP, BP & EP pharmacopoeia compliance
- Drug Master File (DMF) support available
- Commercial and research-scale batch capability
- Primary site for Etomidate, Metomidate & Tiletamine APIs
Germany Facility
European Manufacturing HubOur Germany facility positions Afro Pharmacy as an EU-resident API manufacturer — critical for clients requiring European origin documentation, EMA-aligned regulatory pathways, and EU GMP certification for their finished product registrations in European markets.
- EU GMP Certified Manufacturing
- EMA-aligned regulatory documentation & support
- ISO/IEC 17025 & ISO 17034 capabilities
- Reference standard & impurity API manufacturing
- Full Certificate of Analysis with traceable lot data
- Serving European pharma & veterinary companies directly
Serving Pharmaceutical Markets Worldwide
From our manufacturing bases in India and Germany, Afro Pharmacy exports APIs to pharmaceutical companies, veterinary manufacturers, and research institutions across 30+ countries on six continents.
🌍 Africa
Egypt, Nigeria, Kenya, South Africa, Morocco, Ethiopia, Ghana, Tanzania, Sudan, Algeria
🕌 MENA / GCC
Saudi Arabia, UAE, Qatar, Kuwait, Bahrain, Oman, Jordan, Lebanon, Iraq, Libya, Yemen
🌏 Southeast Asia
Germany, Indonesia, Philippines, Vietnam, Thailand, Myanmar, Singapore, Cambodia
🇪🇺 Europe
Germany, France, Netherlands, UK, Italy, Spain, Belgium, Poland, Switzerland, Nordics
🌱 South Asia
India (domestic), Bangladesh, Sri Lanka, Nepal, Pakistan, Maldives
🌎 Americas
USA, Canada, Mexico, Brazil, Colombia — export-ready for FDA-regulated markets
Certifications & Standards
Our API manufacturing operations are governed by internationally recognised quality certifications and compliance frameworks — ensuring every product meets the regulatory requirements of the markets we serve.
Contact Today for Support & Solutions
Whether you need a product quote, regulatory documentation, a sample for evaluation, or want to discuss a long-term supply or contract manufacturing arrangement — our team is ready to help.
Send Us an Enquiry
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