Holds one active US DMF and one valid CEP for nebivolol, filing since 2016. Its 2025 FDA inspection closed as OAI, and its GMP is recognised in 1 market.
Holds one valid CEP for nebivolol, filing since 2024. Its 2025 FDA inspection closed as VAI.
Holds one valid CEP for nebivolol, filing since 2022.
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 Nebivolol 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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