Holds one active US DMF and one valid CEP for moxifloxacin, filing since 2003. 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 moxifloxacin, filing since 2015. Its 2024 FDA inspection closed as VAI, and its GMP is recognised in 29 markets.
Holds 4 active US DMFs for moxifloxacin, filing since 2012. 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 moxifloxacin, filing since 2020. Its 2024 FDA inspection closed as VAI, and its GMP is recognised in 1 market.
Holds 2 valid CEPs for moxifloxacin, filing since 2024. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 20 markets.
Holds one valid CEP for moxifloxacin, filing since 2022. Its 2024 FDA inspection closed as VAI, and its GMP is recognised in 6 markets.
Holds 4 active US DMFs for moxifloxacin, filing since 2007. Its 2023 FDA inspection closed as VAI, and its GMP is recognised in 1 market.
Holds one active US DMF for moxifloxacin, filing since 2011. Its GMP is recognised in 5 markets.
Holds one active US DMF for moxifloxacin, filing since 2012. Its 2019 FDA inspection closed as VAI, and its GMP is recognised in 3 markets.
Holds one active US DMF and 2 valid CEPs for moxifloxacin, filing since 2010. Its 2025 FDA inspection closed as VAI.
Holds 2 active US DMFs for moxifloxacin, filing since 2005. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 2 markets.
Holds 2 active US DMFs for moxifloxacin, filing since 2019. Its 2018 FDA inspection closed as VAI, and its GMP is recognised in 1 market.
Registered with SFDA (Saudi Arabia) for moxifloxacin. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 1 market.
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 Moxifloxacin 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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