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
- 71335-0720_17b869c0-6c85-4436-a3f1-2b411c2f3367
- Product NDC
- 71335-0720
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- Metformin Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20080417
- 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 (71335-0720-1) · 71335-0720-1
- 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0720-2) · 71335-0720-2
- 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0720-3) · 71335-0720-3
- 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0720-4) · 71335-0720-4
- 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0720-5) · 71335-0720-5
- 15 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0720-6) · 71335-0720-6
- 45 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0720-7) · 71335-0720-7
- 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0720-8) · 71335-0720-8
- 20 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0720-9) · 71335-0720-9
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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