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
- 68462-520_75378e1b-a55d-48ee-9a0a-cd82d2fb78a0
- Product NDC
- 68462-520
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- metformin hydrochloride
- Labeler
- GLENMARK PHARMACEUTICALS INC., USA
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20191125
- Source listing expiry
- 20271231
Source-listed ingredients
- METFORMIN HYDROCHLORIDE — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-520-01) · 68462-520-01
- 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-520-05) · 68462-520-05
- 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-520-10) · 68462-520-10
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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