Holds one active US DMF for bupropion, filing since 2014. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 15 markets.
Holds one active US DMF for bupropion, filing since 2014. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 15 markets.
Holds one active US DMF for bupropion, filing since 2024. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 19 markets.
Holds one active US DMF for bupropion, filing since 2023. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 30 markets.
Holds one active US DMF for bupropion, filing since 2008. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 18 markets.
Holds one active US DMF for bupropion, filing since 2005. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 2 markets.
Holds 4 active US DMFs for bupropion, filing since 2014. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 6 markets.
Holds 2 active US DMFs for bupropion, filing since 2021. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 7 markets.
Holds one active US DMF for bupropion, filing since 2017. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 25 markets.
Holds 4 active US DMFs for bupropion, filing since 2005. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 1 market.
Holds 2 active US DMFs for bupropion, filing since 2006. Its 2025 FDA inspection closed as VAI.
Holds one active US DMF for bupropion, filing since 2013. Its 2026 FDA inspection closed as VAI, and its GMP is recognised in 1 market.
Holds one active US DMF for bupropion, filing since 2020. Its 2023 FDA inspection closed as NAI.
Holds 2 active US DMFs for bupropion, filing since 2024. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 2 markets.
Holds 4 active US DMFs for bupropion, filing since 2006. Its 2022 FDA inspection closed as VAI.
This page filters the worldwide Bupropion 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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