Holds 2 active US DMFs for cefdinir, filing since 2012. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 1 market.
Holds 2 active US DMFs for cefdinir, filing since 2012. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 1 market.
Holds one active US DMF for cefdinir, filing since 2004. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 30 markets.
Holds one active US DMF for cefdinir, filing since 2006. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 3 markets.
Holds 2 active US DMFs for cefdinir, filing since 2006. Its 2025 FDA inspection closed as VAI.
Holds one active US DMF for cefdinir, filing since 2011. Its GMP is recognised in 6 markets.
Registered with SFDA (Saudi Arabia) for cefdinir.
Registered with PMDA (Japan) for cefdinir.
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 Cefdinir 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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