NDC 71335-1834 – Metformin Hydrochloride

Metformin Hydrochloride 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1834

Product details

Brand name
Metformin Hydrochloride
Generic name
Metformin Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA203769
Marketed since
February 1, 2015
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
71335-1834-025 TABLET in 1 BOTTLE (71335-1834-0)Apr 29, 2021
71335-1834-130 TABLET in 1 BOTTLE (71335-1834-1)Apr 29, 2021
71335-1834-260 TABLET in 1 BOTTLE (71335-1834-2)Apr 29, 2021
71335-1834-3100 TABLET in 1 BOTTLE (71335-1834-3)Apr 29, 2021
71335-1834-4120 TABLET in 1 BOTTLE (71335-1834-4)Apr 29, 2021
71335-1834-590 TABLET in 1 BOTTLE (71335-1834-5)Apr 29, 2021
71335-1834-628 TABLET in 1 BOTTLE (71335-1834-6)Apr 29, 2021
71335-1834-756 TABLET in 1 BOTTLE (71335-1834-7)Apr 29, 2021
71335-1834-8180 TABLET in 1 BOTTLE (71335-1834-8)Apr 29, 2021
71335-1834-910 TABLET in 1 BOTTLE (71335-1834-9)Apr 29, 2021

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