Holds one active US DMF and one valid CEP for terbinafine, filing since 2005. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 23 markets.
Holds one active US DMF and one valid CEP for terbinafine, filing since 2005. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 23 markets.
Holds one active US DMF and one valid CEP for terbinafine, filing since 2002. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 26 markets.
Holds one active US DMF and one valid CEP for terbinafine, filing since 2007. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 26 markets.
Holds one active US DMF and 4 valid CEPs for terbinafine, filing since 2004. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 34 markets.
Holds 4 active US DMFs and one valid CEP for terbinafine, filing since 2005. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 1 market.
Holds one active US DMF and one valid CEP for terbinafine, filing since 2005. Its 2025 FDA inspection closed as VAI.
Holds one active US DMF for terbinafine, filing since 2005.
Holds one active US DMF for terbinafine, filing since 2023. Its 2024 FDA inspection closed as VAI.
Holds 2 active US DMFs for terbinafine, filing since 2017. Its 2018 FDA inspection closed as VAI, and its GMP is recognised in 1 market.
Holds 2 active US DMFs for terbinafine, filing since 2022.
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 Terbinafine 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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