Glipizide

Product NDC

50436-6463

11-digit product format

504366463

Labeler code

50436

Product ID

50436-6463_2838f077-c250-40ba-a153-3cc93e6b6a91

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Glipizide

Dosage form

TABLET

Route

ORAL

Labeler

Unit Dose Services

Application

ANDA074223

Marketing category

ANDA

Marketing start

1995-02-27

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