Glipizide

Product NDC

70518-0288

11-digit product format

705180288

Labeler code

70518

Product ID

70518-0288_837446d3-93c2-9c0d-e053-2a91aa0ad133

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

2017-03-07

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

2020-12-31

Current FDA listing

Historical FDA.report record