Glyburide

Product NDC

59115-012

11-digit product format

591150012

Labeler code

59115

Product ID

59115-012_f2e6f347-50f7-4f73-bb81-6ca39e66093c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Glyburide

Dosage form

TABLET

Route

ORAL

Labeler

Hikma Pharmaceutical

Application

ANDA075890

Marketing category

ANDA

Marketing start

2003-08-01

Marketing end

0000-00-00

Substance

GLYBURIDE

Active strength

6 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