Glipizide

Product NDC

68788-7250

11-digit product format

687887250

Labeler code

68788

Product ID

68788-7250_85e6d37c-5c0c-4fff-a49a-6b9004739c0d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Glipizide

Dosage form

TABLET

Route

ORAL

Labeler

Preferred Pharmaceuticals Inc.

Application

ANDA074223

Marketing category

ANDA

Marketing start

2018-08-27

Marketing end

0000-00-00

Substance

GLIPIZIDE

Active strength

10 mg/1

Pharmacologic classes

Sulfonylurea [EPC],Sulfonylurea Compounds [CS]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record