NDC 71335-2533 – Metformin Hydrochloride

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

Human Prescription Drug

Product NDC71335-2533

Product details

Brand name
Metformin Hydrochloride
Generic name
Metformin Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA209882
Marketed since
May 17, 2021
Listing expires
December 31, 2026
Pharmacologic class
Biguanide

Active ingredients

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

Package NDC codes (9)

Package NDCDescriptionSince
71335-2533-01000 TABLET, FILM COATED in 1 BOTTLE (71335-2533-0)Dec 10, 2024
71335-2533-160 TABLET, FILM COATED in 1 BOTTLE (71335-2533-1)Dec 10, 2024
71335-2533-2100 TABLET, FILM COATED in 1 BOTTLE (71335-2533-2)Dec 10, 2024
71335-2533-330 TABLET, FILM COATED in 1 BOTTLE (71335-2533-3)Dec 10, 2024
71335-2533-4120 TABLET, FILM COATED in 1 BOTTLE (71335-2533-4)Dec 10, 2024
71335-2533-590 TABLET, FILM COATED in 1 BOTTLE (71335-2533-5)Dec 10, 2024
71335-2533-628 TABLET, FILM COATED in 1 BOTTLE (71335-2533-6)Dec 10, 2024
71335-2533-756 TABLET, FILM COATED in 1 BOTTLE (71335-2533-7)Dec 10, 2024
71335-2533-8180 TABLET, FILM COATED in 1 BOTTLE (71335-2533-8)Dec 10, 2024

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