NDC 71335-2224 – Metformin Hydrochloride

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

Human Prescription Drug

Product NDC71335-2224

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 (10)

Package NDCDescriptionSince
71335-2224-025 TABLET, FILM COATED in 1 BOTTLE (71335-2224-0)Apr 3, 2024
71335-2224-130 TABLET, FILM COATED in 1 BOTTLE (71335-2224-1)Aug 29, 2023
71335-2224-260 TABLET, FILM COATED in 1 BOTTLE (71335-2224-2)Sep 20, 2023
71335-2224-3100 TABLET, FILM COATED in 1 BOTTLE (71335-2224-3)Nov 16, 2023
71335-2224-4120 TABLET, FILM COATED in 1 BOTTLE (71335-2224-4)Apr 3, 2024
71335-2224-590 TABLET, FILM COATED in 1 BOTTLE (71335-2224-5)Apr 3, 2024
71335-2224-628 TABLET, FILM COATED in 1 BOTTLE (71335-2224-6)Apr 3, 2024
71335-2224-756 TABLET, FILM COATED in 1 BOTTLE (71335-2224-7)Apr 3, 2024
71335-2224-8180 TABLET, FILM COATED in 1 BOTTLE (71335-2224-8)Sep 18, 2023
71335-2224-910 TABLET, FILM COATED in 1 BOTTLE (71335-2224-9)Apr 3, 2024

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