Ezetimibe

Product NDC

49884-228

11-digit product format

498840228

Labeler code

49884

Product ID

49884-228_9f4d2295-5729-4cf3-b191-76e78df2caf8

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ezetimibe

Dosage form

TABLET

Route

ORAL

Labeler

Par Pharmaceutical Inc

Application

ANDA078560

Marketing category

ANDA

Marketing start

2016-12-12

Marketing end

2020-03-31

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

0000-00-00

Current FDA listing

Historical FDA.report record