NDC 65862-008 – Metformin Hydrochloride

Metformin Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

Product NDC65862-008

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
65862-008-01100 TABLET, FILM COATED in 1 BOTTLE (65862-008-01)Jan 14, 2005
65862-008-05500 TABLET, FILM COATED in 1 BOTTLE (65862-008-05)Jan 14, 2005
65862-008-33300 TABLET, FILM COATED in 1 BOTTLE (65862-008-33)Jan 14, 2005
65862-008-454500 TABLET, FILM COATED in 1 BOTTLE (65862-008-45)Jan 14, 2005
65862-008-5050 TABLET, FILM COATED in 1 BOTTLE (65862-008-50)Jan 14, 2005
65862-008-6060 TABLET, FILM COATED in 1 BOTTLE (65862-008-60)Jan 14, 2005
65862-008-9090 TABLET, FILM COATED in 1 BOTTLE (65862-008-90)Jan 14, 2005
65862-008-991000 TABLET, FILM COATED in 1 BOTTLE (65862-008-99)Jan 14, 2005

Recalls mentioning this NDC

Other Metformin hydrochloride products