Holds one active US DMF for quinapril, filing since 2004. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 30 markets.
Holds one active US DMF for quinapril, filing since 2004. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 30 markets.
Holds one active US DMF for quinapril, filing since 2003. Its 2023 FDA inspection closed as VAI, and its GMP is recognised in 1 market.
Holds one active US DMF and one valid CEP for quinapril, filing since 2005. Its 2025 FDA inspection closed as VAI.
Holds one active US DMF for quinapril, filing since 2006. Its 2026 FDA inspection closed as VAI, and its GMP is recognised in 1 market.
Holds one active US DMF and one valid CEP for quinapril, filing since 2006. Its 2025 FDA inspection closed as OAI, and its GMP is recognised in 1 market.
Registered with DAV (Vietnam) for quinapril. Its GMP is recognised in 1 market.
The names are listed below. The filings, inspection history and GMP certificates behind each one are available with a free account.
Open the full list with a free accountContract manufacturers make to order rather than holding their own filing for this molecule.
The order is set by active filings weighted by regulator, inspection outcomes and their recency, breadth of GMP recognition, and evidence of real exports, less any open risk flags. Every factor appears on the card it produced. Read the full method.
Tell us which markets you need to file in. These suppliers come back tiered for those markets, with the price corridor and an RFI sheet.
Start for freeFixed-dose combinations containing quinapril. Each page leads with the verified API makers of every component.