Holds one active US DMF for fesoterodine, filing since 2012. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 30 markets.
Holds one active US DMF for fesoterodine, filing since 2012. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 18 markets.
Holds 2 active US DMFs for fesoterodine, filing since 2012. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 6 markets.
Holds one active US DMF for fesoterodine, filing since 2012. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 25 markets.
Holds one active US DMF for fesoterodine, filing since 2012. Its 2025 FDA inspection closed as NAI.
Holds 2 active US DMFs for fesoterodine, filing since 2018. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 1 market.
Holds 2 active US DMFs for fesoterodine, filing since 2012. Its 2023 FDA inspection closed as VAI, and its GMP is recognised in 1 market.
Holds one active US DMF for fesoterodine, filing since 2021. Its GMP is recognised in 1 market.
This page filters the worldwide Fesoterodine 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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