Glipizide

Product NDC

68071-1557

11-digit product format

680711557

Labeler code

68071

Product ID

68071-1557_7cb42daf-0f54-ca6f-e053-2a91aa0ac9b6

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Glipizide

Dosage form

TABLET, FILM COATED, EXTENDED RELEASE

Route

ORAL

Labeler

NuCare Pharmaceuticals,Inc.

Application

ANDA076467

Marketing category

ANDA

Marketing start

2006-04-01

Marketing end

0000-00-00

Substance

GLIPIZIDE

Active strength

3 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