Cetirizine Hydrochloride

Product NDC

0904-5879

11-digit product format

009045879

Labeler code

0904

Product ID

0904-5879_2dfc1eee-f18b-476c-98b1-75c88e194b03

Type

HUMAN OTC DRUG

Nonproprietary name

Cetirizine Hydrochloride

Dosage form

TABLET, CHEWABLE

Route

ORAL

Labeler

Major Pharmaceuticals

Application

ANDA078692

Marketing category

ANDA

Marketing start

2008-02-14

Marketing end

2019-08-17

Substance

CETIRIZINE HYDROCHLORIDE

Active strength

10 mg/1

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record