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
- 80425-0591_5647163f-4654-233e-e063-6394a90a8fad
- Product NDC
- 80425-0591
- Form
- TABLET, FILM COATED
- Composition / generic term
- metformin hydrochloride
- Labeler
- Advanced Rx of Tennessee, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260710
- Source listing expiry
- 20271231
Source-listed ingredients
- METFORMIN HYDROCHLORIDE — 1000 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0591-1) · 80425-0591-1
- 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0591-2) · 80425-0591-2
- 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0591-3) · 80425-0591-3
- 108 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0591-4) · 80425-0591-4
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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