NDC 71335-1835 – Metformin Hydrochloride

Metformin Hydrochloride 850 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1835

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 (6)

Package NDCDescriptionSince
71335-1835-160 TABLET in 1 BOTTLE (71335-1835-1)Apr 29, 2021
71335-1835-230 TABLET in 1 BOTTLE (71335-1835-2)Apr 29, 2021
71335-1835-3120 TABLET in 1 BOTTLE (71335-1835-3)Apr 29, 2021
71335-1835-490 TABLET in 1 BOTTLE (71335-1835-4)Apr 29, 2021
71335-1835-5100 TABLET in 1 BOTTLE (71335-1835-5)Apr 29, 2021
71335-1835-6180 TABLET in 1 BOTTLE (71335-1835-6)Apr 29, 2021

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