Holds one active US DMF for rifamycin, filing since 2008. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 30 markets.
Holds one active US DMF for rifamycin, filing since 2008. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 30 markets.
Holds 3 active US DMFs and one valid CEP for rifamycin, filing since 2021.
Holds one active US DMF for rifamycin, filing since 2021. Its 2023 FDA inspection closed as NAI.
Holds 3 active US DMFs for rifamycin, filing since 2009. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 3 markets.
Holds 4 active US DMFs for rifamycin, filing since 2010. Its 2025 FDA inspection closed as VAI.
Holds one valid CEP for rifamycin, filing since 2026. Its 2021 FDA inspection closed as VAI, and its GMP is recognised in 2 markets.
Holds one active US DMF for rifamycin, filing since 2014.
Registered with DAV (Vietnam) for rifamycin. Its GMP is recognised in 1 market.
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 rifamycin and what filings they hold.
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