Holds one active US DMF for eptifibatide, filing since 2012. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 3 markets.
Holds one active US DMF for eptifibatide, filing since 2012. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 3 markets.
Holds one active US DMF for eptifibatide, filing since 2017. Its 2024 FDA inspection closed as VAI, and its GMP is recognised in 2 markets.
Holds one active US DMF for eptifibatide, filing since 2013. Its 2023 FDA inspection closed as VAI, and its GMP is recognised in 1 market.
Holds one active US DMF for eptifibatide, filing since 2010.
Holds one active US DMF for eptifibatide, filing since 2025.
Holds one active US DMF for eptifibatide, filing since 2012.
Holds one active US DMF for eptifibatide, filing since 2026.
Registered with SFDA (Saudi Arabia) for eptifibatide. Its 2024 FDA inspection closed as VAI.
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 Eptifibatide manufacturer list to companies based in China. 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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