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
- 72789-561_5839abcb-bd26-3d0c-e063-6394a90a4886
- Product NDC
- 72789-561
- Form
- TABLET, FILM COATED
- Composition / generic term
- METFORMIN HYDROCHLORIDE
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250825
- Source listing expiry
- 20271231
Source-listed ingredients
- METFORMIN HYDROCHLORIDE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-561-20) · 72789-561-20
- 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-561-30) · 72789-561-30
- 42 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-561-42) · 72789-561-42
- 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-561-60) · 72789-561-60
- 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-561-90) · 72789-561-90
- 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-561-93) · 72789-561-93
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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