Holds 2 active US DMFs and 2 valid CEPs for paroxetine, filing since 2006. Its 2025 FDA inspection closed as OAI, and its GMP is recognised in 1 market.
EDQM certificate database
FDA, List of Drug Master Files
Holds 2 active US DMFs and 2 valid CEPs for paroxetine, filing since 2006. Its 2025 FDA inspection closed as OAI, and its GMP is recognised in 1 market.
Holds one active US DMF for paroxetine, filing since 2024. Its 2024 FDA inspection closed as VAI.
Holds one active US DMF for paroxetine, filing since 2025. Its 2024 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 Paroxetine manufacturer list to companies based in China. 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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