Glyburide

Product NDC

51079-873

11-digit product format

510790873

Labeler code

51079

Product ID

51079-873_9aee2e05-bb49-7a7a-e053-2995a90af0ed

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Glyburide

Dosage form

TABLET

Route

ORAL

Labeler

Mylan Institutional Inc.

Application

ANDA074388

Marketing category

ANDA

Marketing start

1996-07-30

Marketing end

2020-11-30

Substance

GLYBURIDE

Active strength

5 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