NDC 80425-0591 – Metformin Hydrochloride

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

Human Prescription Drug

Product NDC80425-0591

Product details

Brand name
Metformin Hydrochloride
Generic name
Metformin hydrochloride
Labeler
Advanced Rx of Tennessee, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA075973
Marketed since
July 10, 2026
Listing expires
December 31, 2027
Pharmacologic class
Biguanide

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
80425-0591-130 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0591-1)Jul 10, 2026
80425-0591-260 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0591-2)Jul 10, 2026
80425-0591-390 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0591-3)Jul 10, 2026
80425-0591-4108 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0591-4)Jul 10, 2026

Other Metformin hydrochloride products