Holds one active US DMF for lenvatinib, filing since 2021. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 1 market.
Holds one active US DMF for lenvatinib, filing since 2026. Its GMP is recognised in 4 markets.
Holds one active US DMF for lenvatinib, filing since 2025. Its 2021 FDA inspection closed as VAI.
Registered with SFDA (Saudi Arabia) for lenvatinib. 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 Lenvatinib 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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