Holds one active US DMF and one valid CEP for famotidine, filing since 1999. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 26 markets.
Holds one active US DMF and 2 valid CEPs for famotidine, filing since 2011. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 18 markets.
Holds one active US DMF and one valid CEP for famotidine, filing since 2021. Its 2024 FDA inspection closed as VAI, and its GMP is recognised in 4 markets.
Holds one active US DMF and one valid CEP for famotidine, filing since 2005. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 25 markets.
Holds 2 valid CEPs for famotidine, filing since 2025. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 19 markets.
Holds 2 active US DMFs for famotidine, filing since 2021. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 6 markets.
Holds one active US DMF for famotidine, filing since 2021. Its 2024 FDA inspection closed as NAI.
Holds one active US DMF and 2 valid CEPs for famotidine, filing since 2008. Its 2025 FDA inspection closed as OAI, and its GMP is recognised in 6 markets.
Holds one active US DMF and one valid CEP for famotidine, filing since 2023. Its 2025 FDA inspection closed as VAI.
Holds 2 active US DMFs for famotidine, filing since 2022. Its 2024 FDA inspection closed as VAI.
Holds one active US DMF for famotidine, filing since 2021. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 2 markets.
Registered with SFDA (Saudi Arabia) for famotidine. Its GMP is recognised in 7 markets.
Holds one valid CEP for famotidine, filing since 2023. Its GMP is recognised in 1 market.
Holds one active US DMF for famotidine, filing since 2023.
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 Famotidine 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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