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 active US DMF 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.
The names are listed below. Ask Fred about the filings, inspection history and GMP certificates on record for each manufacturer.
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.
Ask Fred which manufacturers are on record for propofol and what filings they hold.
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