Glipizide

Product NDC

70518-0115

11-digit product format

705180115

Labeler code

70518

Product ID

70518-0115_9f4d81c8-cb1f-5700-e053-2a95a90a4158

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

glipizide

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA074550

Marketing category

ANDA

Marketing start

2017-01-11

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

2021-12-31

Current FDA listing

Historical FDA.report record