NDC 50090-7877 – Metformin Hydrochloride

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

Human Prescription Drug

Product NDC50090-7877

Product details

Brand name
Metformin Hydrochloride
Generic name
Metformin Hydrochloride
Labeler
A-S Medication Solutions
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA213320
Marketed since
August 25, 2025
Listing expires
December 31, 2027
Pharmacologic class
Biguanide

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
50090-7877-060 TABLET, FILM COATED in 1 BOTTLE (50090-7877-0)Feb 2, 2026
50090-7877-2100 TABLET, FILM COATED in 1 BOTTLE (50090-7877-2)Feb 2, 2026
50090-7877-330 TABLET, FILM COATED in 1 BOTTLE (50090-7877-3)Feb 2, 2026
50090-7877-490 TABLET, FILM COATED in 1 BOTTLE (50090-7877-4)Feb 2, 2026
50090-7877-5180 TABLET, FILM COATED in 1 BOTTLE (50090-7877-5)Feb 2, 2026

Other Metformin hydrochloride products