NDC 51655-120 – Glimepiride

Glimepiride 4 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC51655-120

Product details

Brand name
Glimepiride
Generic name
Glimepiride
Labeler
Northwind Health Company, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078181
Marketed since
December 29, 2014
Listing expires
December 31, 2027
Pharmacologic class
Sulfonylurea

Active ingredients

Uses, dosage, side effects and warnings for Glimepiride →

Package NDC codes (2)

Package NDCDescriptionSince
51655-120-2690 TABLET in 1 BOTTLE, PLASTIC (51655-120-26)Dec 6, 2022
51655-120-5230 TABLET in 1 BOTTLE, DISPENSING (51655-120-52)Dec 29, 2014

Recalls mentioning this NDC

Other Glimepiride products