Glimepiride

Product NDC

50436-7074

11-digit product format

504367074

Labeler code

50436

Product ID

50436-7074_674ef5b8-2fe7-48b0-b77a-7ab86c6054c3

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Glimepiride

Dosage form

TABLET

Route

ORAL

Labeler

Unit Dose Services

Application

ANDA077091

Marketing category

ANDA

Marketing start

2005-10-06

Marketing end

0000-00-00

Substance

GLIMEPIRIDE

Active strength

4 mg/1

Pharmacologic classes

Sulfonylurea [EPC],Sulfonylurea Compounds [CS]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record