Holds one active US DMF and one valid CEP for nebivolol, filing since 2007. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 15 markets.
Holds one active US DMF and one valid CEP for nebivolol, filing since 2009. Its 2026 FDA inspection closed as NAI, and its GMP is recognised in 20 markets.
Holds one active US DMF and 2 valid CEPs for nebivolol, filing since 2016. Its 2024 FDA inspection closed as VAI, and its GMP is recognised in 29 markets.
Holds 4 active US DMFs for nebivolol, filing since 2011. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 6 markets.
Holds one active US DMF and one valid CEP for nebivolol, filing since 2024. Its GMP is recognised in 21 markets.
Holds one active US DMF for nebivolol, filing since 2014. Its 2019 FDA inspection closed as VAI, and its GMP is recognised in 2 markets.
Holds 2 active US DMFs for nebivolol, filing since 2011. Its 2023 FDA inspection closed as VAI, and its GMP is recognised in 1 market.
Holds one active US DMF for nebivolol, filing since 2021.
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 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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