NDC 71335-9683 – Metformin Hydrochloride

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

Human Prescription Drug

Product NDC71335-9683

Product details

Brand name
Metformin Hydrochloride
Generic name
Metformin Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA076756
Marketed since
August 6, 2020
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
71335-9683-160 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9683-1)Apr 11, 2023
71335-9683-230 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9683-2)Apr 11, 2023
71335-9683-3100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9683-3)Apr 11, 2023
71335-9683-490 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9683-4)Apr 11, 2023
71335-9683-5120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9683-5)Apr 11, 2023
71335-9683-615 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9683-6)Apr 11, 2023
71335-9683-745 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9683-7)Apr 11, 2023
71335-9683-8180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9683-8)Apr 11, 2023
71335-9683-920 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-9683-9)Apr 11, 2023

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