United States · FDA National Drug Code directory
Metformin HCl
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
- 72789-192_5683dd49-29a1-2b76-e063-6294a90a3c5b
- Product NDC
- 72789-192
- Form
- TABLET
- Composition / generic term
- Metformin HCl
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170206
- 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 in 1 BOTTLE, PLASTIC (72789-192-20) · 72789-192-20
- 21 TABLET in 1 BOTTLE, PLASTIC (72789-192-21) · 72789-192-21
- 30 TABLET in 1 BOTTLE, PLASTIC (72789-192-30) · 72789-192-30
- 60 TABLET in 1 BOTTLE, PLASTIC (72789-192-60) · 72789-192-60
- 180 TABLET in 1 BOTTLE, PLASTIC (72789-192-93) · 72789-192-93
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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