NDC 76385-128 – Metformin hydrochloride

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

Human Prescription Drug 2 recalls

Product NDC76385-128

Product details

Brand name
Metformin hydrochloride
Generic name
Metformin hydrochloride
Labeler
UNICHEM PHARMACEUTICALS (USA), INC.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA207427
Marketed since
July 17, 2018
Listing expires
December 31, 2027
Pharmacologic class
Biguanide

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
76385-128-01100 TABLET, EXTENDED RELEASE in 1 BOTTLE (76385-128-01)Jul 17, 2018
76385-128-101000 TABLET, EXTENDED RELEASE in 1 BOTTLE (76385-128-10)Jul 17, 2018
76385-128-50500 TABLET, EXTENDED RELEASE in 1 BOTTLE (76385-128-50)Jul 25, 2019

Recalls mentioning this NDC

Other Metformin hydrochloride products