Holds 3 active US DMFs for lenalidomide, filing since 2017. Its 2024 FDA inspection closed as VAI, and its GMP is recognised in 2 markets.
Holds one active US DMF for lenalidomide, filing since 2021. Its GMP is recognised in 4 markets.
Holds one active US DMF for lenalidomide, filing since 2021. Its 2019 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 Lenalidomide 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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