GLIPIZIDE

Product NDC

51655-105

11-digit product format

516550105

Labeler code

51655

Product ID

51655-105_ab615d0d-ab59-4d12-badd-670a882954e6

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

GLIPIZIDE

Dosage form

TABLET

Route

ORAL

Labeler

Northwind Pharmaceuticals

Application

ANDA077820

Marketing category

ANDA

Marketing start

2014-12-29

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

2019-12-31

Current FDA listing

Historical FDA.report record