Glipizide

Product NDC

65862-888

11-digit product format

658620888

Labeler code

65862

Product ID

65862-888_963bea5a-dda1-4ce0-9ee4-35e40eb82606

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Glipizide

Dosage form

TABLET, EXTENDED RELEASE

Route

ORAL

Labeler

Aurobindo Pharma Limited

Application

ANDA206928

Marketing category

ANDA

Marketing start

2017-05-12

Marketing end

2020-08-31

Substance

GLIPIZIDE

Active strength

3 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