Holds one active US DMF and one valid CEP for etomidate, filing since 2013. Its 2026 FDA inspection closed as VAI, and its GMP is recognised in 1 market.
Holds one active US DMF and one valid CEP for etomidate, filing since 2013. Its 2026 FDA inspection closed as VAI, and its GMP is recognised in 1 market.
Holds one active US DMF for etomidate, filing since 2019. Its 2024 FDA inspection closed as VAI, and its GMP is recognised in 19 markets.
Holds one active US DMF for etomidate, filing since 2007. Its 2024 FDA inspection closed as VAI, and its GMP is recognised in 2 markets.
Holds one active US DMF for etomidate, filing since 2002. Its 2021 FDA inspection closed as VAI.
Registered with DAV (Vietnam) for etomidate. Its GMP is recognised in 1 market.
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