Ranked API manufacturers
01 India
Makes the APIFinished dose
Credentials confirmed against the regulator files on 25 July 2026
Holds 3 active US DMFs and one valid CEP for ceftazidime, filing since 2009. 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
02 Italy
Makes the APIFinished dose
Credentials confirmed against the regulator files on 25 July 2026
Holds 12 active US DMFs and one valid CEP for ceftazidime, filing since 1998. Its 2023 FDA inspection closed as VAI, and its GMP is recognised in 12 markets.
Last FDA inspection
2023 · VAI
GMP recognised in
12 markets
03 Switzerland
Makes the APIFinished dose
Credentials confirmed against the regulator files on 25 July 2026
Holds one active US DMF and one valid CEP for ceftazidime, filing since 2002. Its 2024 FDA inspection closed as VAI, and its GMP is recognised in 29 markets.
Last FDA inspection
2024 · VAI
GMP recognised in
29 markets
04 Sweden
Makes the APIFinished dose
Credentials confirmed against the regulator files on 25 July 2026
Holds one active US DMF for ceftazidime, filing since 2023. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 48 markets.
Last FDA inspection
2025 · NAI
GMP recognised in
48 markets
05 United Kingdom
Makes the APIFinished dose
Its 2026 FDA inspection closed as NAI, and its GMP is recognised in 37 markets.
Last FDA inspection
2026 · NAI
GMP recognised in
37 markets
06 China
Makes the APIFinished dose
Credentials confirmed against the regulator files on 25 July 2026
Holds one active US DMF for ceftazidime, filing since 2006. Its 2023 FDA inspection closed as VAI, and its GMP is recognised in 5 markets.
Last FDA inspection
2023 · VAI
GMP recognised in
5 markets
Credentials confirmed against the regulator files on 25 July 2026
Holds one active US DMF for ceftazidime, filing since 2012. Its GMP is recognised in 6 markets.
Last FDA inspection
Not established
GMP recognised in
6 markets
Credentials confirmed against the regulator files on 25 July 2026
Holds one active US DMF for ceftazidime, filing since 2011. Its 2015 FDA inspection closed as VAI, and its GMP is recognised in 2 markets.
Last FDA inspection
2015 · VAI
GMP recognised in
2 markets
09 South Korea
Makes the API
Holds one valid CEP for ceftazidime, filing since 2023. Its GMP is recognised in 1 market.
Last FDA inspection
Not established
GMP recognised in
1 markets
10 Vietnam
Makes the APIFinished dose
Registered with DAV (Vietnam) for ceftazidime. Its GMP is recognised in 1 market.
Last FDA inspection
Not established
GMP recognised in
1 markets
How this listing is sourced Regulator filings, warehouse snapshot 9 July 2026
View profile 11 Vietnam
Makes the APIFinished dose
Registered with DAV (Vietnam) for ceftazidime. Its GMP is recognised in 3 markets.
Last FDA inspection
Not established
GMP recognised in
3 markets
How this listing is sourced Regulator filings, warehouse snapshot 9 July 2026
View profile 12 Vietnam
Makes the APIFinished dose
Registered with DAV (Vietnam) for ceftazidime. Its GMP is recognised in 1 market.
Last FDA inspection
Not established
GMP recognised in
1 markets
How this listing is sourced Regulator filings, warehouse snapshot 9 July 2026
View profile 13 Vietnam
Makes the APIFinished dose
Registered with DAV (Vietnam) for ceftazidime. Its GMP is recognised in 1 market.
Last FDA inspection
Not established
GMP recognised in
1 markets
How this listing is sourced Regulator filings, warehouse snapshot 9 July 2026
View profile 14 Vietnam
Makes the APIFinished dose
Registered with DAV (Vietnam) for ceftazidime. Its GMP is recognised in 2 markets.
Last FDA inspection
Not established
GMP recognised in
2 markets
How this listing is sourced Regulator filings, warehouse snapshot 9 July 2026
View profile 11 more manufacturers hold filings for ceftazidime
The names are listed below. The filings, inspection history and GMP certificates behind
each one are available with a free account.
Open the full list with a free account Contract manufacturers (7)
Contract manufacturers make to order rather than holding their own filing for this
molecule.
Finished-dose makers (102)
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.