Glipizide

Product NDC

70518-0456

11-digit product format

705180456

Labeler code

70518

Product ID

70518-0456_86d3ffad-5beb-700a-e053-2991aa0a1cc9

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Glipizide

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA076467

Marketing category

ANDA

Marketing start

2017-04-24

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

2020-12-31

Current FDA listing

Historical FDA.report record