United States · FDA National Drug Code directory
Metformin hydrochloride ER
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
- 72789-106_560a7b34-48b7-1ac4-e063-6394a90a0016
- Product NDC
- 72789-106
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- Metformin hydrochloride
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180628
- Source listing expiry
- 20271231
Source-listed ingredients
- METFORMIN HYDROCHLORIDE — 750 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-106-01) · 72789-106-01
- 500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-106-82) · 72789-106-82
- 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-106-90) · 72789-106-90
- 180 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-106-93) · 72789-106-93
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 →