Glipizide

Product NDC

68071-2181

11-digit product format

680712181

Labeler code

68071

Product ID

68071-2181_43c9d391-6581-02c6-e054-00144ff8d46c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Glipizide

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

ANDA076467

Marketing category

ANDA

Marketing start

2015-07-02

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