Glimepiride

Product NDC

55154-5070

11-digit product format

551545070

Labeler code

55154

Product ID

55154-5070_5a27121b-7a52-4e45-920f-0380b5c4c7f0

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

glimepiride

Dosage form

TABLET

Route

ORAL

Labeler

Cardinal Health

Application

ANDA077624

Marketing category

ANDA

Marketing start

2010-11-04

Marketing end

0000-00-00

Substance

GLIMEPIRIDE

Active strength

2 mg/1

Pharmacologic classes

Sulfonylurea [EPC],Sulfonylurea Compounds [CS]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record