United States · FDA National Drug Code directory
METFORMIN HYDROCHLORIDE EXTENDED RELEASE
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
- 72789-009_560798a8-34ca-25ac-e063-6294a90ad854
- Product NDC
- 72789-009
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- Metformin Hydrochloride
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160512
- Source listing expiry
- 20271231
Source-listed ingredients
- METFORMIN HYDROCHLORIDE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-009-30) · 72789-009-30
- 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-009-60) · 72789-009-60
- 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-009-90) · 72789-009-90
- 180 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-009-93) · 72789-009-93
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 →