Molecules / Glutamic Acid

Glutamic Acid API manufacturers

CAS 56-86-0 Updated 9 July 2026
5
manufacturers with an active filing 4 of them hold a US DMF or a CEP
9
shortage records on file across 1 countries
251
finished-dose makers across 17 regulators
Showing 5 of 5 manufacturers This list is ranked on evidence. Placement cannot be purchased.

Ranked API manufacturers

01

Ajinomoto

Japan
Makes the API
Credentials confirmed against the regulator files on 25 July 2026

Holds one active US DMF and one valid CEP for glutamic acid, filing since 2006. Its 2025 FDA inspection closed as VAI, and its GMP is recognised in 4 markets.

US DMF
1 active
CEP
1 valid
Last FDA inspection
2025 · VAI
GMP recognised in
4 markets
02

Taenaka Kogyo

Japan
Makes the API
Credentials confirmed against the regulator files on 25 July 2026

Holds one active US DMF and one valid CEP for glutamic acid, filing since 1991. Its 2024 FDA inspection closed as VAI.

US DMF
1 active
CEP
1 valid
Last FDA inspection
2024 · VAI
GMP recognised in
Not established
03

Otsuka Pharmaceutical India

India
Makes the APIFinished dose

Registered with DAV (Vietnam) for glutamic acid. Its 2025 FDA inspection closed as NAI, and its GMP is recognised in 36 markets.

US DMF
None on file
CEP
None on file
Last FDA inspection
2025 · NAI
GMP recognised in
36 markets
How this listing is sourced Regulator filings, warehouse snapshot 9 July 2026
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04

AMINO

Germany
Makes the API
Credentials confirmed against the regulator files on 25 July 2026

Holds one valid CEP for glutamic acid, filing since 2026. Its 2022 FDA inspection closed as VAI, and its GMP is recognised in 2 markets.

US DMF
None on file
CEP
1 valid
Last FDA inspection
2022 · VAI
GMP recognised in
2 markets
How this listing is sourced EDQM certificate database
View profile

2 more manufacturers hold filings for glutamic acid

The names are listed below. The filings, inspection history and GMP certificates behind each one are available with a free account.

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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

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