United States · FDA National Drug Code directory
L-Glutamine
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 70954-417_0635706e-180e-435e-92cf-c85e0ca4f7e0
- Product NDC
- 70954-417
- Form
- POWDER, FOR SOLUTION
- Composition / generic term
- L-Glutamine
- Labeler
- ANI Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240711
- Source listing expiry
- 20261231
Source-listed ingredients
- GLUTAMINE — 5 g/1
These values do not establish equivalence or a dose recommendation.
Packages
- 60 PACKET in 1 CARTON (70954-417-20) / 1 POWDER, FOR SOLUTION in 1 PACKET (70954-417-10) · 70954-417-20
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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