Cetirizine Hydrochloride

Product NDC

0536-4088

11-digit product format

005364088

Labeler code

0536

Product ID

0536-4088_a78dc390-30b6-4362-a088-022d76121e83

Type

HUMAN OTC DRUG

Nonproprietary name

Cetirizine hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Rugby Laboratories, Inc.

Application

ANDA078780

Marketing category

ANDA

Marketing start

2012-03-23

Marketing end

2020-02-28

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