Ezetimibe

Product NDC

60687-284

11-digit product format

606870284

Labeler code

60687

Product ID

60687-284_76df86ec-b396-ab8e-e053-2a91aa0ad10d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ezetimibe

Dosage form

TABLET

Route

ORAL

Labeler

American Health Packaging

Application

ANDA078560

Marketing category

ANDA

Marketing start

2017-01-26

Marketing end

2019-09-30

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