Glipizide

Product NDC

50436-6302

11-digit product format

504366302

Labeler code

50436

Product ID

50436-6302_04ea34ab-7652-4fc3-97b0-c8bb9baac9d5

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Glipizide

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

Unit Dose Services

Application

ANDA076467

Marketing category

ANDA

Marketing start

2003-11-19

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