Cetirizine Hydrochloride

Product NDC

0179-8302

11-digit product format

001798302

Labeler code

0179

Product ID

0179-8302_7b09840f-5839-588a-e053-2a91aa0ad033

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

5 mg/1

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record