CHILDRENS ALLERGY

Product NDC

37808-884

11-digit product format

378080884

Labeler code

37808

Product ID

37808-884_d32cb9f9-a1c4-4fb2-ab33-9932c4765ed7

Type

HUMAN OTC DRUG

Nonproprietary name

cetirizine Hydrochloride

Dosage form

SOLUTION

Route

ORAL

Labeler

H E B

Application

ANDA090254

Marketing category

ANDA

Marketing start

2010-11-01

Marketing end

0000-00-00

Substance

CETIRIZINE HYDROCHLORIDE

Active strength

5 mg/5mL

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record