Holds one valid CEP for olmesartan medoxomil, filing since 2024. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 15 markets.
Holds one valid CEP for olmesartan medoxomil, filing since 2024. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 15 markets.
Holds 2 valid CEPs for olmesartan medoxomil, filing since 2024. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 23 markets.
Holds 2 valid CEPs for olmesartan medoxomil, filing since 2025. Its 2024 FDA inspection closed as VAI, and its GMP is recognised in 29 markets.
Holds one valid CEP for olmesartan medoxomil, filing since 2026. Its 2026 FDA inspection closed as NAI, and its GMP is recognised in 20 markets.
Holds 2 valid CEPs for olmesartan medoxomil, filing since 2026. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 18 markets.
Holds one valid CEP for olmesartan medoxomil, filing since 2025. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 26 markets.
Holds 2 valid CEPs for olmesartan medoxomil, filing since 2023. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 20 markets.
Holds one valid CEP for olmesartan medoxomil, filing since 2023. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 25 markets.
Holds 2 valid CEPs for olmesartan medoxomil, filing since 2025. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 1 market.
Holds one valid CEP for olmesartan medoxomil, filing since 2024. Its 2023 FDA inspection closed as NAI, and its GMP is recognised in 2 markets.
Holds one valid CEP for olmesartan medoxomil, filing since 2025. Its 2025 FDA inspection closed as VAI.
Holds 4 valid CEPs for olmesartan medoxomil, filing since 2024.
Holds 2 valid CEPs for olmesartan medoxomil, filing since 2025.
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 Olmesartan Medoxomil 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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