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
- 71335-0293_1210ee1b-4a39-4f60-af08-02eeca33dfca
- Product NDC
- 71335-0293
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- METFORMIN HYDROCHLORIDE
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160512
- Source listing expiry
- 20261231
Source-listed ingredients
- METFORMIN HYDROCHLORIDE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0293-1) · 71335-0293-1
- 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0293-2) · 71335-0293-2
- 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0293-3) · 71335-0293-3
- 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0293-4) · 71335-0293-4
- 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0293-5) · 71335-0293-5
- 15 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0293-6) · 71335-0293-6
- 45 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0293-7) · 71335-0293-7
- 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0293-8) · 71335-0293-8
- 20 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0293-9) · 71335-0293-9
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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