Glipizide

Product NDC

70518-0389

11-digit product format

705180389

Labeler code

70518

Product ID

70518-0389_842bdfe0-bea3-6b2f-e053-2a91aa0af857

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Glipizide

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA076159

Marketing category

ANDA

Marketing start

2017-04-04

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