All Day Allergy

Product NDC

68016-279

11-digit product format

680160279

Labeler code

68016

Product ID

68016-279_a24a6ac8-cf80-4a2d-b873-6b9d8e611c1d

Type

HUMAN OTC DRUG

Nonproprietary name

Cetirizine Hydrochloride

Dosage form

CAPSULE

Route

ORAL

Labeler

Chain Drug Consortium, LLC

Application

NDA022429

Marketing category

NDA

Marketing start

2013-06-01

Marketing end

2020-12-31

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