Holds 2 active US DMFs for rilpivirine, filing since 2015. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 13 markets.
Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 10 markets.
Holds 2 active US DMFs for rilpivirine, filing since 2015. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 6 markets.
Holds 2 active US DMFs for rilpivirine, filing since 2017. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 34 markets.
Holds one active US DMF for rilpivirine, filing since 2022. Its GMP is recognised in 4 markets.
Holds one active US DMF for rilpivirine, filing since 2024. Its 2023 FDA inspection closed as VAI, and its GMP is recognised in 1 market.
Holds one active US DMF for rilpivirine, filing since 2013. Its 2025 FDA inspection closed as VAI.
Holds 4 active US DMFs for rilpivirine, filing since 2016. Its 2023 FDA inspection closed as VAI, and 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 rilpivirine and what filings they hold.
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