Glimepiride

Product NDC

50436-7075

11-digit product format

504367075

Labeler code

50436

Product ID

50436-7075_1dcb7264-1f3b-432d-aaa6-ecf822cdac58

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

1 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