NDC 70518-1951 – Metformin Hydrochloride

Metformin Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC70518-1951

Product details

Brand name
Metformin Hydrochloride
Generic name
Metformin Hydrochloride
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203769
Marketed since
March 12, 2019
Marketing end
January 1, 2027
Pharmacologic class
Biguanide

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
70518-1951-290 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1951-2)Jun 1, 2025
70518-1951-330 TABLET, FILM COATED in 1 BLISTER PACK (70518-1951-3)Oct 28, 2025

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