Holds 2 active US DMFs for memantine, filing since 2010. Its 2024 FDA inspection closed as VAI, and its GMP is recognised in 29 markets.
Holds 2 active US DMFs for memantine, filing since 2010. Its 2024 FDA inspection closed as VAI, and its GMP is recognised in 29 markets.
Holds one active US DMF for memantine, filing since 2007. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 26 markets.
Holds one active US DMF for memantine, filing since 2007. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 30 markets.
Holds one active US DMF for memantine, filing since 2009. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 18 markets.
Holds 2 active US DMFs for memantine, filing since 2011. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 6 markets.
Holds one active US DMF for memantine, filing since 2021. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 25 markets.
Holds one active US DMF for memantine, filing since 2011. Its 2023 FDA inspection closed as VAI.
Holds 2 active US DMFs for memantine, filing since 2015. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 1 market.
Holds one active US DMF for memantine, filing since 2011. Its 2019 FDA inspection closed as VAI, and its GMP is recognised in 3 markets.
Holds one active US DMF for memantine, filing since 2007.
Registered with SFDA (Saudi Arabia) for memantine. Its 2026 FDA inspection closed as VAI, and its GMP is recognised in 13 markets.
Holds one active US DMF for memantine, filing since 2007. Its 2025 FDA inspection closed as VAI.
Holds 2 active US DMFs for memantine, filing since 2008. Its 2023 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 Memantine 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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