United States · FDA National Drug Code directory
Metformin HCl
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
- 49483-620_2dc48b61-581f-fe5c-e063-6394a90aa557
- Product NDC
- 49483-620
- Form
- TABLET, FILM COATED
- Composition / generic term
- Metformin HCl
- Labeler
- TIME CAP LABORATORIES, INC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20161114
- 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, PLASTIC (49483-620-01) · 49483-620-01
- 1000 TABLET, FILM COATED in 1 PACKAGE (49483-620-10) · 49483-620-10
- 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49483-620-50) · 49483-620-50
- 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49483-620-81) · 49483-620-81
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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