Holds one active US DMF and one valid CEP for levocetirizine, filing since 2007. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 26 markets.
Holds one active US DMF and one valid CEP for levocetirizine, filing since 2007. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 26 markets.
Holds 2 active US DMFs and 2 valid CEPs for levocetirizine, filing since 2008. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 2 markets.
Holds one active US DMF for levocetirizine, filing since 2007. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 34 markets.
Holds 2 active US DMFs for levocetirizine, filing since 2009. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 7 markets.
Holds 2 active US DMFs for levocetirizine, filing since 2009. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 1 market.
Holds 2 active US DMFs for levocetirizine, filing since 2008. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 1 market.
Holds 2 active US DMFs for levocetirizine, filing since 2007. Its 2024 FDA inspection closed as VAI.
Holds 2 active US DMFs for levocetirizine, filing since 2012. Its 2022 FDA inspection closed as VAI.
Holds 2 active US DMFs for levocetirizine, filing since 2019. Its 2018 FDA inspection closed as VAI, and its GMP is recognised in 1 market.
Registered with SFDA (Saudi Arabia) for levocetirizine.
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 Levocetirizine 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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