Glyburide

Product NDC

50436-6409

11-digit product format

504366409

Labeler code

50436

Product ID

50436-6409_a2ba73c1-2ace-4497-8bcd-3adb40f05eaf

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Glyburide

Dosage form

TABLET

Route

ORAL

Labeler

Unit Dose Services

Application

ANDA074388

Marketing category

ANDA

Marketing start

1995-08-30

Marketing end

0000-00-00

Substance

GLYBURIDE

Active strength

5 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