Glipizide

Product NDC

68788-9918

11-digit product format

687889918

Labeler code

68788

Product ID

68788-9918_c74c2da7-458b-484d-bd65-96258270a3c8

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Glipizide

Dosage form

TABLET

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA074305

Marketing category

ANDA

Marketing start

2012-01-30

Marketing end

0000-00-00

Substance

GLIPIZIDE

Active strength

5 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