# L-glutamine

NDC: 31722-483
Generic name: L-glutamine
Labeler / Manufacturer: Camber Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SOLUTION
Routes: ORAL
Marketing started: 20260526

FDA application: ANDA219722

## Active ingredients

- GLUTAMINE: 5 g/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"31722-483"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-483
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4d99b233-992f-4adb-aaab-ef0021a3807f