Childrens All Day Allergy

Product NDC

37205-826

11-digit product format

372050826

Labeler code

37205

Product ID

37205-826_62e795b9-af6c-4847-a0de-3e4d29e67c90

Type

HUMAN OTC DRUG

Nonproprietary name

cetirizine hydrochloride

Dosage form

LIQUID

Route

ORAL

Labeler

Cardinal Health

Application

ANDA090254

Marketing category

ANDA

Marketing start

2009-09-29

Marketing end

0000-00-00

Substance

CETIRIZINE HYDROCHLORIDE

Active strength

5 mg/5mL

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record