NDC 68462-521 – Metformin Hydrochloride

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

Human Prescription Drug 1 recall

Product NDC68462-521

Product details

Brand name
Metformin Hydrochloride
Generic name
Metformin hydrochloride
Labeler
GLENMARK PHARMACEUTICALS INC., USA
Dosage form
Tablet, Film Coated, Extended Release
Route
Oral
Marketing category
ANDA · ANDA212969
Marketed since
November 25, 2019
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
68462-521-01100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-521-01)Nov 25, 2019
68462-521-05500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-521-05)Nov 25, 2019
68462-521-9090 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-521-90)Nov 25, 2019

Recalls mentioning this NDC

Other Metformin hydrochloride products