Holds one active US DMF and one valid CEP for montelukast, filing since 2019. Its 2024 FDA inspection closed as VAI, and its GMP is recognised in 6 markets.
Holds one active US DMF and one valid CEP for montelukast, filing since 2018. Its 2024 FDA inspection closed as VAI.
Holds one active US DMF for montelukast, filing since 2014. Its 2023 FDA inspection closed as VAI.
Holds one active US DMF for montelukast, filing since 2014.
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 Montelukast 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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