United States · FDA National Drug Code directory
Metformin Hydrochloride
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
- 11788-037_0f811364-27e3-4449-b343-8d97f4c9a87f
- Product NDC
- 11788-037
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- Metformin Hydrochloride Extended-Release Tablets
- Labeler
- AiPing Pharmaceutical, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20251215
- Source listing expiry
- 20271231
Source-listed ingredients
- METFORMIN HYDROCHLORIDE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (11788-037-60) · 11788-037-60
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →