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
- 42385-977_6a8acfd4-a0e4-41e3-bdb9-c0ceebfa0ffc
- Product NDC
- 42385-977
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- METFORMIN HYDROCHLORIDE
- Labeler
- Laurus Labs Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20231006
- 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, EXTENDED RELEASE in 1 BOTTLE (42385-977-01) · 42385-977-01
- 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (42385-977-05) · 42385-977-05
- 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (42385-977-11) · 42385-977-11
- 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (42385-977-18) · 42385-977-18
- 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (42385-977-30) · 42385-977-30
- 15 BLISTER PACK in 1 CARTON (42385-977-72) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK · 42385-977-72
- 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (42385-977-90) · 42385-977-90
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 →