Cetirizine Hydrochloride

Product NDC

49348-939

11-digit product format

493480939

Labeler code

49348

Product ID

49348-939_3c2dd452-9a10-416c-91e6-170ba0723fed

Type

HUMAN OTC DRUG

Nonproprietary name

Cetirizine Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

McKesson

Application

ANDA078862

Marketing category

ANDA

Marketing start

2011-08-01

Marketing end

0000-00-00

Substance

CETIRIZINE HYDROCHLORIDE

Active strength

10 mg/1

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record