Glipizide

Product NDC

70518-1124

11-digit product format

705181124

Labeler code

70518

Product ID

70518-1124_906ffda2-e010-4b0f-e053-2995a90abb3c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Glipizide

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA074223

Marketing category

ANDA

Marketing start

2018-04-19

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

2020-12-31

Current FDA listing

Historical FDA.report record