FDA NDC Directory · JSON-LD · Markdown

L-glutamine

NDC 31722-483 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SOLUTION

Labeler / ManufacturerCamber Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA219722
Dosage form / routePOWDER, FOR SOLUTION · ORAL
Active ingredientsGLUTAMINE (5 g/1)
Marketing started20260526
Package count1

External sources

Source: openFDA. Public-domain (CC0).