Glipizide

Product NDC

70518-0358

11-digit product format

705180358

Labeler code

70518

Product ID

70518-0358_83ebb894-afd8-bd99-e053-2a91aa0af2b6

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Glipizide

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA074305

Marketing category

ANDA

Marketing start

2017-03-23

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