Ezetimibe

Product NDC

50090-3402

11-digit product format

500903402

Labeler code

50090

Product ID

50090-3402_66482340-2525-4170-9281-0289de6245c1

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Ezetimibe

Dosage form

TABLET

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA208332

Marketing category

ANDA

Marketing start

2017-06-12

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

2019-12-31

Current FDA listing

Historical FDA.report record