Glipizide

Product NDC

68645-151

11-digit product format

686450151

Labeler code

68645

Product ID

68645-151_fe05d092-bf3b-4a96-be0a-8a499c4224c8

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Glipizide

Dosage form

TABLET

Route

ORAL

Labeler

Legacy Pharmaceutical Packaging, LLC

Application

ANDA074305

Marketing category

ANDA

Marketing start

1995-04-07

Marketing end

2019-04-30

Substance

GLIPIZIDE

Active strength

10 mg/1

Pharmacologic classes

Sulfonylurea [EPC],Sulfonylurea Compounds [CS]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record