NDC 71335-0886 – Metformin Hydrochloride

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

Human Prescription Drug

Product NDC71335-0886

Product details

Brand name
Metformin Hydrochloride
Generic name
Metformin hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA201991
Marketed since
March 1, 2013
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
71335-0886-160 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0886-1)Aug 20, 2018
71335-0886-230 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0886-2)Dec 27, 2021
71335-0886-3100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0886-3)Jul 17, 2018
71335-0886-490 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0886-4)Aug 7, 2018
71335-0886-5120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0886-5)Jun 28, 2018
71335-0886-615 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0886-6)Dec 27, 2021
71335-0886-745 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0886-7)Dec 27, 2021
71335-0886-8180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0886-8)Dec 27, 2021
71335-0886-920 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0886-9)Dec 27, 2021

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