GlyBURIDE

Product NDC

67253-461

11-digit product format

672530461

Labeler code

67253

Product ID

67253-461_6a545ff2-035a-4cce-bd27-b6851f7d2e91

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

GlyBURIDE

Dosage form

TABLET

Route

ORAL

Labeler

Par Pharmaceutical

Application

ANDA074591

Marketing category

ANDA

Marketing start

1997-12-22

Marketing end

0000-00-00

Substance

GLYBURIDE

Active strength

3 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