Glipizide

Product NDC

63187-234

11-digit product format

631870234

Labeler code

63187

Product ID

63187-234_5aca7caf-5b01-4230-b287-97316191a30b

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Glipizide

Dosage form

TABLET

Route

ORAL

Labeler

Proficient Rx LP

Application

ANDA074305

Marketing category

ANDA

Marketing start

1995-04-07

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

2020-12-31

Current FDA listing

Historical FDA.report record