Glipizide

Product NDC

50090-2076

11-digit product format

500902076

Labeler code

50090

Product ID

50090-2076_e8b79b32-8563-455d-bd72-367ce9f4d992

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

glipizide

Dosage form

TABLET

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA074550

Marketing category

ANDA

Marketing start

2011-07-18

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