Ranked API manufacturers
Credentials confirmed against the regulator files on 25 July 2026
Holds one valid CEP for cefuroxime axetil, filing since 2024. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 1 market.
Last FDA inspection
2025 · NAI
GMP recognised in
1 markets
Credentials confirmed against the regulator files on 25 July 2026
Holds 2 valid CEPs for cefuroxime axetil, filing since 2024. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 3 markets.
Last FDA inspection
2025 · VAI
GMP recognised in
3 markets
Credentials confirmed against the regulator files on 25 July 2026
Holds one valid CEP for cefuroxime axetil, filing since 2025.
Last FDA inspection
Not established
GMP recognised in
Not established
04 South Korea
Makes the API
Credentials confirmed against the regulator files on 25 July 2026
Holds one valid CEP for cefuroxime axetil, filing since 2011. Its GMP is recognised in 2 markets.
Last FDA inspection
Not established
GMP recognised in
2 markets
Credentials confirmed against the regulator files on 25 July 2026
Holds one valid CEP for cefuroxime axetil, filing since 2025.
Last FDA inspection
Not established
GMP recognised in
Not established
Credentials confirmed against the regulator files on 25 July 2026
Holds one valid CEP for cefuroxime axetil, filing since 2024.
Last FDA inspection
Not established
GMP recognised in
Not established
07 India
Makes the APIFinished dose
Registered with SFDA (Saudi Arabia) for cefuroxime axetil. Its GMP is recognised in 6 markets.
Last FDA inspection
Not established
GMP recognised in
6 markets
How this listing is sourced Regulator filings, warehouse snapshot 9 July 2026
View profile Registered with SFDA (Saudi Arabia) for cefuroxime axetil.
Last FDA inspection
Not established
GMP recognised in
Not established
How this listing is sourced Regulator filings, warehouse snapshot 9 July 2026
View profile 5 more manufacturers hold filings for cefuroxime axetil
The names are listed below. Ask Fred about the filings, inspection history and GMP
certificates on record for each manufacturer.
Chat with Fred, your AI analyst Finished-dose makers (42)
How this list is built
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.
Every factor appears on the card it produced.
Read the full method.
- Active US DMFs
- FDA, List of Drug Master Files
- Valid CEPs
- EDQM certificate database
- Inspection outcomes
- FDA inspection classifications
- GMP certificates
- EudraGMDP and national regulators
- Price band
-
Customs export unit values for 2025. These are export values rather than
contract prices for regulated-market grade material, which are higher.