Glipizide

Product NDC

68071-3141

11-digit product format

680713141

Labeler code

68071

Product ID

68071-3141_49b0543b-5e1a-50ee-e054-00144ff8d46c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Glipizide

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

NuCare Pharmaceuticals Inc,

Application

ANDA076159

Marketing category

ANDA

Marketing start

2016-12-21

Marketing end

0000-00-00

Substance

GLIPIZIDE

Active strength

10 mg/1

Pharmacologic classes

Sulfonylurea [EPC],Sulfonylurea Compounds [CS]

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record