glyBURIDE

Product NDC

55700-576

11-digit product format

557000576

Labeler code

55700

Product ID

55700-576_3038f35a-0fa3-42e9-a310-c12b602b6c4d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

glyBURIDE

Dosage form

TABLET

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA203581

Marketing category

ANDA

Marketing start

2018-01-05

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