Holds one active US DMF and 4 valid CEPs for fenofibrate, filing since 2002. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 18 markets.
EDQM certificate database
FDA, List of Drug Master Files
Holds one active US DMF and 4 valid CEPs for fenofibrate, filing since 2002. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 18 markets.
Holds one active US DMF and one valid CEP for fenofibrate, filing since 2009. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 3 markets.
Holds 2 active US DMFs for fenofibrate, filing since 2012. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 6 markets.
Holds one active US DMF and one valid CEP for fenofibrate, filing since 2022. Its 2019 FDA inspection closed as VAI, and its GMP is recognised in 1 market.
Holds one active US DMF for fenofibrate, filing since 2008. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 30 markets.
Holds 2 valid CEPs for fenofibrate, filing since 2014. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 19 markets.
Holds one valid CEP for fenofibrate, filing since 2026. Its 2024 FDA inspection closed as VAI, and its GMP is recognised in 6 markets.
Holds one active US DMF for fenofibrate, filing since 2024.
Holds one valid CEP for fenofibrate, filing since 2025.
Holds one active US DMF for fenofibrate, filing since 1994.
The names are listed below. The filings, inspection history and GMP certificates behind each one are available with a free account.
This page filters the worldwide Fenofibrate manufacturer list to companies based in India. 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. 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