NDC 71335-2466 – Metformin Hydrochloride

Metformin Hydrochloride 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2466

Product details

Brand name
Metformin Hydrochloride
Generic name
Metformin hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA213320
Marketed since
January 19, 2023
Listing expires
December 31, 2026
Pharmacologic class
Biguanide

Active ingredients

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

Package NDC codes (10)

Package NDCDescriptionSince
71335-2466-025 TABLET in 1 BOTTLE (71335-2466-0)Aug 16, 2024
71335-2466-130 TABLET in 1 BOTTLE (71335-2466-1)Aug 16, 2024
71335-2466-260 TABLET in 1 BOTTLE (71335-2466-2)Aug 16, 2024
71335-2466-3100 TABLET in 1 BOTTLE (71335-2466-3)Aug 16, 2024
71335-2466-4120 TABLET in 1 BOTTLE (71335-2466-4)Aug 16, 2024
71335-2466-590 TABLET in 1 BOTTLE (71335-2466-5)Aug 16, 2024
71335-2466-628 TABLET in 1 BOTTLE (71335-2466-6)Aug 16, 2024
71335-2466-756 TABLET in 1 BOTTLE (71335-2466-7)Aug 16, 2024
71335-2466-8180 TABLET in 1 BOTTLE (71335-2466-8)Aug 16, 2024
71335-2466-910 TABLET in 1 BOTTLE (71335-2466-9)Aug 16, 2024

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