Holds one active US DMF and 2 valid CEPs for oxybutynin, filing since 2009. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 3 markets.
EDQM certificate database
FDA, List of Drug Master Files
Holds one active US DMF and 2 valid CEPs for oxybutynin, filing since 2009. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 3 markets.
Holds one valid CEP for oxybutynin, filing since 2022. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 10 markets.
Holds one active US DMF for oxybutynin, filing since 2006. Its 2025 FDA inspection closed as VAI.
Holds 2 active US DMFs for oxybutynin, filing since 2010. Its 2025 FDA inspection closed as VAI.
The names are listed below. The filings, inspection history and GMP certificates behind each one are available with a free account.
Open the full list with a free accountThis page filters the worldwide Oxybutynin 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.
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