Cetirizine Hydrochloride

Product NDC

0536-1041

11-digit product format

005361041

Labeler code

0536

Product ID

0536-1041_2befc0ab-dc50-42d2-9e84-8102961035b8

Type

HUMAN OTC DRUG

Nonproprietary name

Cetirizine Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Rugby Laboratories

Application

ANDA078317

Marketing category

ANDA

Marketing start

2007-12-27

Marketing end

2020-04-30

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