Holds one active US DMF for tedizolid, filing since 2024. Its 2023 FDA inspection closed as VAI, and its GMP is recognised in 1 market.
Holds one active US DMF for tedizolid, filing since 2024. Its 2023 FDA inspection closed as VAI, and its GMP is recognised in 1 market.
Holds one active US DMF for tedizolid, filing since 2024. Its GMP is recognised in 4 markets.
Holds one active US DMF for tedizolid, filing since 2025.
Holds one active US DMF for tedizolid, filing since 2024.
Holds one active US DMF for tedizolid, filing since 2024.
This page filters the worldwide Tedizolid 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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