Glimepiride

Product NDC

51079-425

11-digit product format

510790425

Labeler code

51079

Product ID

51079-425_96b1794a-244b-80a0-e053-2a95a90a929c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

glimepiride

Dosage form

TABLET

Route

ORAL

Labeler

Mylan Institutional Inc.

Application

ANDA077624

Marketing category

ANDA

Marketing start

2006-03-27

Marketing end

2020-05-31

Substance

GLIMEPIRIDE

Active strength

2 mg/1

Pharmacologic classes

Sulfonylurea [EPC],Sulfonylurea Compounds [CS]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record