NDC 71335-2568 – Metformin Hydrochloride

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

Human Prescription Drug

Product NDC71335-2568

Product details

Brand name
Metformin Hydrochloride
Generic name
Metformin Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA217631
Marketed since
October 6, 2023
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
71335-2568-160 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2568-1)Feb 5, 2025
71335-2568-230 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2568-2)Feb 5, 2025
71335-2568-3100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2568-3)Feb 5, 2025
71335-2568-490 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2568-4)Feb 5, 2025
71335-2568-5120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2568-5)Feb 5, 2025
71335-2568-615 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2568-6)Feb 5, 2025
71335-2568-745 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2568-7)Feb 5, 2025
71335-2568-8180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2568-8)Feb 5, 2025
71335-2568-920 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2568-9)Feb 5, 2025

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