NDC 65862-010 – Metformin Hydrochloride

Metformin Hydrochloride 1000 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

Product NDC65862-010

Product details

Brand name
Metformin Hydrochloride
Generic name
Metformin Hydrochloride
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077095
Marketed since
January 14, 2005
Listing expires
December 31, 2027
Pharmacologic class
Biguanide

Active ingredients

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

Package NDC codes (8)

Package NDCDescriptionSince
65862-010-01100 TABLET, FILM COATED in 1 BOTTLE (65862-010-01)Jan 14, 2005
65862-010-05500 TABLET, FILM COATED in 1 BOTTLE (65862-010-05)Jan 14, 2005
65862-010-33300 TABLET, FILM COATED in 1 BOTTLE (65862-010-33)Jan 14, 2005
65862-010-462000 TABLET, FILM COATED in 1 BOTTLE (65862-010-46)Jan 14, 2005
65862-010-5050 TABLET, FILM COATED in 1 BOTTLE (65862-010-50)Jan 14, 2005
65862-010-6060 TABLET, FILM COATED in 1 BOTTLE (65862-010-60)Jan 14, 2005
65862-010-9090 TABLET, FILM COATED in 1 BOTTLE (65862-010-90)Jan 14, 2005
65862-010-991000 TABLET, FILM COATED in 1 BOTTLE (65862-010-99)Jan 14, 2005

Recalls mentioning this NDC

Other Metformin hydrochloride products