Holds 2 active US DMFs and 2 valid CEPs for sumatriptan, filing since 2003. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 26 markets.
EDQM certificate database
FDA, List of Drug Master Files
Holds 2 active US DMFs and 2 valid CEPs for sumatriptan, filing since 2003. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 26 markets.
Holds 4 active US DMFs and one valid CEP for sumatriptan, filing since 2003. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 15 markets.
Holds one active US DMF for sumatriptan, filing since 2010. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 2 markets.
Holds one valid CEP for sumatriptan, filing since 2026. Its 2024 FDA inspection closed as VAI, and its GMP is recognised in 6 markets.
Holds 2 active US DMFs and one valid CEP for sumatriptan, filing since 2007. Its 2025 FDA inspection closed as OAI, and its GMP is recognised in 6 markets.
Holds 2 active US DMFs and 2 valid CEPs for sumatriptan, filing since 2006. Its 2025 FDA inspection closed as VAI.
Holds 4 active US DMFs for sumatriptan, filing since 2009. Its 2023 FDA inspection closed as VAI, and its GMP is recognised in 1 market.
Holds one active US DMF for sumatriptan, filing since 2006.
Holds one active US DMF for sumatriptan, filing since 2008. Its 2025 FDA inspection closed as VAI.
Holds 2 active US DMFs for sumatriptan, filing since 2022. Its 2018 FDA inspection closed as VAI, and its GMP is recognised in 1 market.
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 Sumatriptan 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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