Holds one active US DMF for pomalidomide, filing since 2016. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 23 markets.
Holds one active US DMF for pomalidomide, filing since 2017. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 26 markets.
Holds one active US DMF for pomalidomide, filing since 2016. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 26 markets.
Holds one active US DMF for pomalidomide, filing since 2025. Its 2024 FDA inspection closed as VAI, and its GMP is recognised in 29 markets.
Holds 2 active US DMFs for pomalidomide, filing since 2016. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 15 markets.
Holds one active US DMF for pomalidomide, filing since 2017. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 1 market.
Holds one active US DMF for pomalidomide, filing since 2023. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 34 markets.
Holds 2 active US DMFs for pomalidomide, filing since 2015. Its 2025 FDA inspection closed as VAI.
Registered with SFDA (Saudi Arabia) for pomalidomide.
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 Pomalidomide 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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