NDC 65162-179 – Metformin Hydrochloride

Metformin Hydrochloride 750 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug 4 recalls

Product NDC65162-179

Product details

Brand name
Metformin Hydrochloride
Generic name
Metformin Hydrochloride
Labeler
Amneal Pharmaceuticals LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA078596
Marketed since
February 26, 2010
Listing expires
December 31, 2026
Pharmacologic class
Biguanide

Active ingredients

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

Package NDC codes (4)

Package NDCDescriptionSince
65162-179-0330 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-179-03)Feb 26, 2010
65162-179-0990 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-179-09)Feb 26, 2010
65162-179-10100 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-179-10)Feb 26, 2010
65162-179-50500 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-179-50)Feb 26, 2010

Recalls mentioning this NDC

Other Metformin hydrochloride products