Holds one active US DMF and one valid CEP for aripiprazole, filing since 2015. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 15 markets.
Holds 2 active US DMFs and 2 valid CEPs for aripiprazole, filing since 2009. 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 aripiprazole, filing since 2012. Its 2024 FDA inspection closed as VAI, and its GMP is recognised in 29 markets.
Holds 2 active US DMFs and 2 valid CEPs for aripiprazole, filing since 2009. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 18 markets.
Holds one active US DMF and one valid CEP for aripiprazole, filing since 2006. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 25 markets.
Holds 4 active US DMFs and one valid CEP for aripiprazole, filing since 2009. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 2 markets.
Holds 2 active US DMFs and one valid CEP for aripiprazole, filing since 2015. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 1 market.
Holds 2 active US DMFs for aripiprazole, filing since 2021. Its 2024 FDA inspection closed as VAI, and its GMP is recognised in 19 markets.
Holds one active US DMF and one valid CEP for aripiprazole, filing since 2014. Its GMP is recognised in 21 markets.
Holds one active US DMF and one valid CEP for aripiprazole, filing since 2015. Its 2025 FDA inspection closed as OAI, and its GMP is recognised in 6 markets.
Holds one valid CEP for aripiprazole, filing since 2025. Its 2026 FDA inspection closed as VAI, and its GMP is recognised in 13 markets.
Holds 2 active US DMFs and one valid CEP for aripiprazole, filing since 2011. Its 2025 FDA inspection closed as VAI.
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 Aripiprazole 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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