Holds one active US DMF and 2 valid CEPs for levonorgestrel, filing since 2009. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 30 markets.
Holds one active US DMF for levonorgestrel, filing since 2008. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 34 markets.
Holds one active US DMF for levonorgestrel, filing since 2014. Its 2022 FDA inspection closed as VAI.
Holds 3 active US DMFs for levonorgestrel, filing since 2025. 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.
Open the full list with a free accountThis page filters the worldwide Levonorgestrel 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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