glyBURIDE

Product NDC

70518-1121

11-digit product format

705181121

Labeler code

70518

Product ID

70518-1121_906f7453-58f1-402b-e053-2995a90a8019

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

glyBURIDE

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA203581

Marketing category

ANDA

Marketing start

2018-04-16

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

2020-12-31

Current FDA listing

Historical FDA.report record