All Day Allergy

Product NDC

30142-884

11-digit product format

301420884

Labeler code

30142

Product ID

30142-884_fea35f74-1b94-489a-83f0-d4fdf562d109

Type

HUMAN OTC DRUG

Nonproprietary name

cetirizine Hydrochloride

Dosage form

SOLUTION

Route

ORAL

Labeler

Kroger Company

Application

ANDA090254

Marketing category

ANDA

Marketing start

2011-08-05

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