Glipizide

Product NDC

35356-899

11-digit product format

353560899

Labeler code

35356

Product ID

35356-899_ea93ccfe-e1b2-435f-85ee-b7ed7c004fbd

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Glipizide

Dosage form

TABLET

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA074305

Marketing category

ANDA

Marketing start

1995-04-07

Marketing end

0000-00-00

Substance

GLIPIZIDE

Active strength

10 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