NDC 68180-339 – Metformin Hydrochloride

Metformin Hydrochloride 1000 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug 2 recalls

Product NDC68180-339

Product details

Brand name
Metformin Hydrochloride
Generic name
Metformin Hydrochloride
Labeler
Lupin Pharmaceuticals, Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA091664
Marketed since
February 1, 2016
Listing expires
December 31, 2027
Pharmacologic class
Biguanide

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
68180-339-0990 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-339-09)Feb 1, 2016

Recalls mentioning this NDC

Other Metformin hydrochloride products