Holds one active US DMF and 2 valid CEPs for hydroxychloroquine, filing since 1999. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 19 markets.
Holds one active US DMF and one valid CEP for hydroxychloroquine, filing since 2000. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 25 markets.
Holds 2 active US DMFs and one valid CEP for hydroxychloroquine, filing since 2017. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 13 markets.
Holds one active US DMF and one valid CEP for hydroxychloroquine, filing since 2021. Its 2024 FDA inspection closed as VAI, and its GMP is recognised in 4 markets.
Holds 2 active US DMFs and one valid CEP for hydroxychloroquine, filing since 2023. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 2 markets.
Holds one active US DMF for hydroxychloroquine, filing since 2021. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 26 markets.
Holds one active US DMF for hydroxychloroquine, filing since 2020. Its 2019 FDA inspection closed as NAI.
Holds one active US DMF for hydroxychloroquine, filing since 2022. Its 2025 FDA inspection closed as OAI, and its GMP is recognised in 6 markets.
The names are listed below. The filings, inspection history and GMP certificates behind each one are available with a free account.
Open the full list with a free accountThis page filters the worldwide Hydroxychloroquine 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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