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
- 67877-932_8c7835fa-3f68-4850-b1da-34893bafb485
- Product NDC
- 67877-932
- Form
- TABLET, FILM COATED
- Composition / generic term
- METFORMIN HYDROCHLORIDE
- Labeler
- Ascend Laboratories, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250825
- Source listing expiry
- 20261231
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 (67877-932-01) · 67877-932-01
- 500 TABLET, FILM COATED in 1 BOTTLE (67877-932-05) · 67877-932-05
- 1000 TABLET, FILM COATED in 1 BOTTLE (67877-932-10) · 67877-932-10
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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