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
- 62207-442_556273f5-2d98-8477-e063-6294a90ad8a6
- Product NDC
- 62207-442
- Form
- TABLET
- Composition / generic term
- Metformin Hydrochloride Tablet
- Labeler
- Granules India Ltd
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190704
- 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 in 1 BOTTLE (62207-442-43) · 62207-442-43
- 500 TABLET in 1 BOTTLE (62207-442-47) · 62207-442-47
- 1000 TABLET in 1 BOTTLE (62207-442-49) · 62207-442-49
- 60 TABLET in 1 BOTTLE (62207-442-50) · 62207-442-50
- 90 TABLET in 1 BOTTLE (62207-442-57) · 62207-442-57
- 27916 TABLET in 1 DRUM (62207-442-98) · 62207-442-98
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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