NDC 71335-0720 – Metformin Hydrochloride

Metformin Hydrochloride 500 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC71335-0720

Product details

Brand name
Metformin Hydrochloride
Generic name
Metformin Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA078321
Marketed since
April 17, 2008
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
71335-0720-160 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0720-1)Mar 15, 2018
71335-0720-230 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0720-2)Mar 15, 2018
71335-0720-3100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0720-3)Mar 15, 2018
71335-0720-490 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0720-4)Mar 15, 2018
71335-0720-5120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0720-5)Mar 15, 2018
71335-0720-615 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0720-6)Mar 15, 2018
71335-0720-745 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0720-7)Mar 15, 2018
71335-0720-8180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0720-8)Mar 15, 2018
71335-0720-920 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0720-9)Mar 15, 2018

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