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
- 71335-1833_b8c444a2-3c51-4b13-83f8-386116e9dc79
- Product NDC
- 71335-1833
- Form
- TABLET
- Composition / generic term
- METFORMIN HYDROCHLORIDE
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20150201
- Source listing expiry
- 20261231
Source-listed ingredients
- METFORMIN HYDROCHLORIDE — 1000 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 TABLET in 1 BOTTLE (71335-1833-0) · 71335-1833-0
- 60 TABLET in 1 BOTTLE (71335-1833-1) · 71335-1833-1
- 100 TABLET in 1 BOTTLE (71335-1833-2) · 71335-1833-2
- 30 TABLET in 1 BOTTLE (71335-1833-3) · 71335-1833-3
- 120 TABLET in 1 BOTTLE (71335-1833-4) · 71335-1833-4
- 90 TABLET in 1 BOTTLE (71335-1833-5) · 71335-1833-5
- 28 TABLET in 1 BOTTLE (71335-1833-6) · 71335-1833-6
- 56 TABLET in 1 BOTTLE (71335-1833-7) · 71335-1833-7
- 180 TABLET in 1 BOTTLE (71335-1833-8) · 71335-1833-8
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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