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
- 65862-010_61f56acf-2add-4ee0-ad61-9dc5334cfc6a
- Product NDC
- 65862-010
- Form
- TABLET, FILM COATED
- Composition / generic term
- Metformin Hydrochloride
- Labeler
- Aurobindo Pharma Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20050114
- Source listing expiry
- 20271231
Source-listed ingredients
- METFORMIN HYDROCHLORIDE — 1000 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (65862-010-01) · 65862-010-01
- 500 TABLET, FILM COATED in 1 BOTTLE (65862-010-05) · 65862-010-05
- 300 TABLET, FILM COATED in 1 BOTTLE (65862-010-33) · 65862-010-33
- 2000 TABLET, FILM COATED in 1 BOTTLE (65862-010-46) · 65862-010-46
- 50 TABLET, FILM COATED in 1 BOTTLE (65862-010-50) · 65862-010-50
- 60 TABLET, FILM COATED in 1 BOTTLE (65862-010-60) · 65862-010-60
- 90 TABLET, FILM COATED in 1 BOTTLE (65862-010-90) · 65862-010-90
- 1000 TABLET, FILM COATED in 1 BOTTLE (65862-010-99) · 65862-010-99
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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