NDC 71335-3166 – Metformin Hydrochloride

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

Human Prescription Drug

Product NDC71335-3166

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
February 15, 2024
Listing expires
December 31, 2027
Pharmacologic class
Biguanide

Active ingredients

Uses, dosage, side effects and warnings for Metformin hydrochloride →

Package NDC codes (9)

Package NDCDescriptionSince
71335-3166-160 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3166-1)Aug 4, 2026
71335-3166-230 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3166-2)Aug 4, 2026
71335-3166-3100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3166-3)Aug 4, 2026
71335-3166-490 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3166-4)Aug 4, 2026
71335-3166-5120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3166-5)Aug 4, 2026
71335-3166-615 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3166-6)Aug 4, 2026
71335-3166-745 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3166-7)Aug 4, 2026
71335-3166-8180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3166-8)Aug 4, 2026
71335-3166-920 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3166-9)Aug 4, 2026

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