Glimepiride

Product NDC

63629-1255

11-digit product format

636291255

Labeler code

63629

Product ID

63629-1255_b0e4346c-1b5b-48a5-91dc-3403bc9485ec

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Glimepiride

Dosage form

TABLET

Route

ORAL

Labeler

Bryant Ranch Prepack

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