Ezetimibe

Product NDC

42291-314

11-digit product format

422910314

Labeler code

42291

Product ID

42291-314_affd8326-09bf-51a2-e053-2a95a90abf53

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ezetimibe

Dosage form

TABLET

Route

ORAL

Labeler

AvKARE, Inc.

Application

ANDA208332

Marketing category

ANDA

Marketing start

2017-06-15

Marketing end

0000-00-00

Substance

EZETIMIBE

Active strength

10 mg/1

Pharmacologic classes

Decreased Cholesterol Absorption [PE],Dietary Cholesterol Absorption Inhibitor [EPC]

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record