NDC 71335-1833 – Metformin Hydrochloride

Metformin Hydrochloride 1000 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1833

Product details

Brand name
Metformin Hydrochloride
Generic name
Metformin Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA203769
Marketed since
February 1, 2015
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
71335-1833-01000 TABLET in 1 BOTTLE (71335-1833-0)Apr 29, 2021
71335-1833-160 TABLET in 1 BOTTLE (71335-1833-1)Apr 29, 2021
71335-1833-2100 TABLET in 1 BOTTLE (71335-1833-2)Apr 29, 2021
71335-1833-330 TABLET in 1 BOTTLE (71335-1833-3)Apr 29, 2021
71335-1833-4120 TABLET in 1 BOTTLE (71335-1833-4)Apr 29, 2021
71335-1833-590 TABLET in 1 BOTTLE (71335-1833-5)Apr 29, 2021
71335-1833-628 TABLET in 1 BOTTLE (71335-1833-6)Apr 29, 2021
71335-1833-756 TABLET in 1 BOTTLE (71335-1833-7)Apr 29, 2021
71335-1833-8180 TABLET in 1 BOTTLE (71335-1833-8)Apr 29, 2021

Other Metformin hydrochloride products