Glipizide

Product NDC

63629-3158

11-digit product format

636293158

Labeler code

63629

Product ID

63629-3158_246c7654-2097-4ecc-b316-a65e399eacf0

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Glipizide

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA076467

Marketing category

ANDA

Marketing start

2003-11-07

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

2019-12-31

Current FDA listing

Historical FDA.report record