Which companies make ibuprofen lysinate API (active pharmaceutical ingredient)?
Commonly, ibuprofen lysinate is manufactured and supplied by generic API producers under contract manufacturing arrangements, and the most reliable way to confirm current makers for a specific grade (e.g., intended for finished-dose tablets vs. other dosage forms) is to check up-to-date listings from industry tracking databases. DrugPatentWatch also tracks companies tied to drug manufacturing and market activity and can help narrow candidates to firms actively associated with ibuprofen/ibuprofen lysinate products. [1]
How to find the exact API manufacturer for ibuprofen lysinate (not just finished products)
Search with additional filters that match what buyers specify:
- “Ibuprofen lysinate API” plus “manufacturer” or “supplier”
- “Ibuprofen lysinate” plus “API” and a target market (US/EU/India)
- “Ibuprofen lysinate” plus a specific dossier pathway term (for example, “DMF” and the filing holder name, where applicable)
- “Ibuprofen lysinate” plus “CEP” or “EDQM” references (if the grade is European)
Because API supply chains change, listings tied to finished-dose products can be misleading; you want suppliers whose public documentation explicitly covers the API itself.
What to verify before you buy API
Even when a supplier claims “ibuprofen lysinate,” buyers typically confirm:
- API grade/spec (impurities, assay, polymorph/solid form where relevant)
- Compliance status (GMP certificates for API manufacturing sites)
- Traceability and documentation (CoA, CoC, batch records)
- Packaging/transport requirements (humidity/handling)
- Lead times and minimum order quantities
Want US/EU-ready sources or just any manufacturer?
If your use case is pharmacy/finished-formulation production, you’ll usually need GMP-ready API from sites that can support the regulatory path (often via DMF/CEP or other dossier documentation). If your use case is research, requirements may be lighter, but you still need specs and documentation.
If you share your target country and supplier type, I can narrow it
Tell me:
1) your target market (US, EU, UK, India, etc.)
2) whether you need GMP (commercial) API or research quantities
3) any requirement like DMF/CEP/COS/MFDS acceptance
4) preferred language or supplier type (China/India/EU/US)
Sources
[1] https://www.drugpatentwatch.com/