NDC 62756-142 – Metformin Hydrochloride

Metformin Hydrochloride 500 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug 4 recalls

Product NDC62756-142

Product details

Brand name
Metformin Hydrochloride
Generic name
Metformin Hydrochloride
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA077336
Marketed since
February 9, 2006
Listing expires
December 31, 2027
Pharmacologic class
Biguanide

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
62756-142-01100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-142-01)Feb 9, 2006
62756-142-02500 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-142-02)Feb 9, 2006

Recalls mentioning this NDC

Other Metformin hydrochloride products