NDC 51655-649 – Metformin Hydrochloride

Metformin Hydrochloride 1000 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC51655-649

Product details

Brand name
Metformin Hydrochloride
Generic name
Metformin Hydrochloride
Labeler
Northwind Health Company, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077095
Marketed since
April 1, 2021
Listing expires
December 31, 2027
Pharmacologic class
Biguanide

Active ingredients

Uses, dosage, side effects and warnings for Metformin hydrochloride →

Package NDC codes (3)

Package NDCDescriptionSince
51655-649-2560 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-649-25)Jul 23, 2025
51655-649-2690 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-649-26)Jun 23, 2023
51655-649-5230 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-649-52)Apr 1, 2021

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