Cetirizine Hydrochloride

Product NDC

0179-8301

11-digit product format

001798301

Labeler code

0179

Product ID

0179-8301_7b0964ac-4265-e982-e053-2991aa0a3c99

Type

HUMAN OTC DRUG

Nonproprietary name

Cetirizine Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Kaiser Foundation Hospitals

Application

ANDA077829

Marketing category

ANDA

Marketing start

2013-12-13

Marketing end

2019-11-30

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