Holds one active US DMF for lenalidomide, filing since 2014. Its 2022 FDA inspection closed as NAI, and its GMP is recognised in 13 markets.
Holds one active US DMF for lenalidomide, filing since 2014. Its 2022 FDA inspection closed as NAI, and its GMP is recognised in 13 markets.
Holds 3 active US DMFs for lenalidomide, filing since 2015. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 26 markets.
Holds 2 active US DMFs for lenalidomide, filing since 2017. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 26 markets.
Holds one active US DMF for lenalidomide, filing since 2017. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 23 markets.
Holds one active US DMF for lenalidomide, filing since 2020. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 29 markets.
Holds one active US DMF for lenalidomide, filing since 2020. Its GMP is recognised in 14 markets.
Holds one active US DMF for lenalidomide, filing since 2020. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 18 markets.
Holds one active US DMF for lenalidomide, filing since 2021. Its GMP is recognised in 12 markets.
Holds 2 active US DMFs for lenalidomide, filing since 2016. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 34 markets.
Holds one active US DMF for lenalidomide, filing since 2013. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 25 markets.
Holds one active US DMF for lenalidomide, filing since 2020. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 1 market.
Holds one active US DMF for lenalidomide, filing since 2022. Its 2025 FDA inspection closed as VAI.
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 2025 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.
Registered with SFDA (Saudi Arabia) for lenalidomide. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 13 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.
Registered with SFDA (Saudi Arabia) for lenalidomide. Its 2024 FDA inspection closed as VAI, and its GMP is recognised in 18 markets.
Holds one active US DMF for lenalidomide, filing since 2009. Its 2025 FDA inspection closed as VAI.
Holds 3 active US DMFs for lenalidomide, filing since 2023. 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.
Contract manufacturers make to order rather than holding their own filing for this molecule.
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. Every factor appears on the card it produced. 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| Year | Median | Exporters |
|---|---|---|
| 2025 | $14375.48 | 15 |
| 2024 | $21742.29 | 11 |
| 2023 | $22130.35 | 13 |
| 2022 | $19901.92 | 12 |
US dollars per kilogram, customs export unit values.