Glipizide

Product NDC

55154-0539

11-digit product format

551540539

Labeler code

55154

Product ID

55154-0539_d926cfc7-3bc5-489d-95ae-814c6eee1171

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

glipizide

Dosage form

TABLET, EXTENDED RELEASE

Route

ORAL

Labeler

Cardinal Health

Application

NDA020329

Marketing category

NDA

Marketing start

1994-04-26

Marketing end

0000-00-00

Substance

GLIPIZIDE

Active strength

3 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