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
- 62207-497_5a918a65-96d8-917d-e063-6294a90acc1d
- Product NDC
- 62207-497
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- Metformin Hydrochloride
- Labeler
- Granules India Ltd
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210201
- Source listing expiry
- 20271231
Source-listed ingredients
- METFORMIN HYDROCHLORIDE — 1000 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (62207-497-47) · 62207-497-47
- 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62207-497-54) · 62207-497-54
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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