Glimepiride

Product NDC

68788-6818

11-digit product format

687886818

Labeler code

68788

Product ID

68788-6818_d98981a1-c656-4f09-b505-08cc318dc53e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Glimepiride

Dosage form

TABLET

Route

ORAL

Labeler

Preferred Pharmaceuticals Inc.

Application

ANDA091220

Marketing category

ANDA

Marketing start

2016-11-17

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