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
- 42385-949_4afe5891-539c-4299-a96a-4a6bfcc22407
- Product NDC
- 42385-949
- Form
- TABLET, FILM COATED
- Composition / generic term
- Metformin Hydrochloride
- Labeler
- Laurus Labs Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210517
- 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, FILM COATED in 1 BOTTLE (42385-949-01) · 42385-949-01
- 500 TABLET, FILM COATED in 1 BOTTLE (42385-949-05) · 42385-949-05
- 1000 TABLET, FILM COATED in 1 BOTTLE (42385-949-11) · 42385-949-11
- 180 TABLET, FILM COATED in 1 BOTTLE (42385-949-18) · 42385-949-18
- 10 BLISTER PACK in 1 CARTON (42385-949-19) / 10 TABLET, FILM COATED in 1 BLISTER PACK · 42385-949-19
- 60 TABLET, FILM COATED in 1 BOTTLE (42385-949-60) · 42385-949-60
- 90 TABLET, FILM COATED in 1 BOTTLE (42385-949-90) · 42385-949-90
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →