Holds one active US DMF and one valid CEP for ramipril, filing since 2002. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 26 markets.
Holds one active US DMF and 2 valid CEPs for ramipril, filing since 2004. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 23 markets.
Holds one active US DMF and 4 valid CEPs for ramipril, filing since 2003. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 34 markets.
Holds 2 active US DMFs and one valid CEP for ramipril, filing since 2003. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 2 markets.
Holds one active US DMF for ramipril, filing since 2005. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 30 markets.
Holds one active US DMF for ramipril, filing since 2006. Its GMP is recognised in 5 markets.
Holds one active US DMF and one valid CEP for ramipril, filing since 2004. Its 2025 FDA inspection closed as VAI.
Holds one active US DMF for ramipril, filing since 2006. Its 2026 FDA inspection closed as VAI, and its GMP is recognised in 1 market.
Holds one valid CEP for ramipril, filing since 2019. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 1 market.
Registered with SFDA (Saudi Arabia) for ramipril.
The names are listed below. The filings, inspection history and GMP certificates behind each one are available with a free account.
This page filters the worldwide Ramipril 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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