Holds 2 active US DMFs and one valid CEP for propofol, filing since 2013. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 2 markets.
Holds one active US DMF and one valid CEP for propofol, filing since 1995. Its 2025 FDA inspection closed as VAI.
Holds one active US DMF for propofol, filing since 1994. Its 2024 FDA inspection closed as VAI, and its GMP is recognised in 2 markets.
Holds one valid CEP for propofol, filing since 2025. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 3 markets.
Holds one valid CEP for propofol, filing since 2021. Its 2023 FDA inspection closed as VAI, and its GMP is recognised in 2 markets.
Holds one active US DMF for propofol, filing since 2025. Its GMP is recognised in 4 markets.
Holds one active US DMF for propofol, filing since 1994.
The names are listed below. The filings, inspection history and GMP certificates behind each one are available with a free account.
Contract 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 free