Holds one active US DMF for sacubitril, filing since 2024. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 26 markets.
Holds one active US DMF for sacubitril, filing since 2019. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 29 markets.
Holds 4 active US DMFs for sacubitril, filing since 2017. Its 2024 FDA inspection closed as VAI, and its GMP is recognised in 4 markets.
Holds 2 active US DMFs for sacubitril, filing since 2024. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 6 markets.
Holds one active US DMF for sacubitril, filing since 2025. Its 2024 FDA inspection closed as VAI, and its GMP is recognised in 6 markets.
Holds one active US DMF for sacubitril, filing since 2019. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 18 markets.
Holds 2 active US DMFs for sacubitril, filing since 2019. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 13 markets.
Holds 4 active US DMFs for sacubitril, filing since 2021. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 14 markets.
Holds one active US DMF for sacubitril, filing since 2025. Its 2024 FDA inspection closed as VAI, and its GMP is recognised in 3 markets.
Holds one active US DMF for sacubitril, filing since 2018. Its 2025 FDA inspection closed as NAI.
Holds 2 active US DMFs for sacubitril, filing since 2023. Its 2024 FDA inspection closed as VAI, and its GMP is recognised in 2 markets.
Registered with SFDA (Saudi Arabia) for sacubitril. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 3 markets.
Holds 2 active US DMFs for sacubitril, filing since 2019. Its 2019 FDA inspection closed as VAI, and its GMP is recognised in 2 markets.
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 Sacubitril 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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