Holds one active US DMF for tenofovir disoproxil, filing since 2011. Its 2023 FDA inspection closed as VAI, and its GMP is recognised in 1 market.
Holds one active US DMF for tenofovir disoproxil, filing since 2011. Its 2023 FDA inspection closed as VAI, and its GMP is recognised in 1 market.
Holds one active US DMF for tenofovir disoproxil, filing since 2019. Its GMP is recognised in 4 markets.
Holds one active US DMF for tenofovir disoproxil, filing since 2016. Its 2019 FDA inspection closed as VAI, and its GMP is recognised in 1 market.
Holds one active US DMF for tenofovir disoproxil, filing since 2023. Its 2024 FDA inspection closed as VAI.
Holds one active US DMF for tenofovir disoproxil, filing since 2014. Its 2025 FDA inspection closed as VAI.
Holds 2 active US DMFs for tenofovir disoproxil, filing since 2016. Its GMP is recognised in 1 market.
This page filters the worldwide Tenofovir Disoproxil 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.
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