Holds one active US DMF for eribulin, filing since 2022. Its 2024 FDA inspection closed as NAI.
Holds one active US DMF for eribulin, filing since 2022. Its 2024 FDA inspection closed as NAI.
Holds one active US DMF for eribulin, filing since 2023. Its 2024 FDA inspection closed as NAI.
Holds one active US DMF for eribulin, filing since 2021. Its 2024 FDA inspection closed as NAI.
Holds one active US DMF for eribulin, filing since 2023. Its 2025 FDA inspection closed as VAI.
Holds 5 active US DMFs for eribulin, filing since 2021.
Holds one active US DMF for eribulin, filing since 2020. Its GMP is recognised in 1 market.
Holds one active US DMF for eribulin, filing since 2020.
Holds 2 active US DMFs for eribulin, filing since 2024.
Holds one active US DMF for eribulin, filing since 2022.
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 Eribulin 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.
Tell us which markets you need to file in. These suppliers come back tiered for those markets, with the price corridor and an RFI sheet.
Start for free