Holds one active US DMF and one valid CEP for capecitabine, filing since 2013. Its 2019 FDA inspection closed as VAI, and its GMP is recognised in 2 markets.
Holds one active US DMF for capecitabine, filing since 2013.
Holds one valid CEP for capecitabine, filing since 2023.
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 Capecitabine 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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