Childrens Cetirizine Hydrochloride

Product NDC

68071-4433

11-digit product format

680714433

Labeler code

68071

Product ID

68071-4433_6c45610f-f367-2b43-e053-2a91aa0a1892

Type

HUMAN OTC DRUG

Nonproprietary name

Cetirizine Hydrochloride

Dosage form

SOLUTION

Route

ORAL

Labeler

NuCare Pharmaceuticals,Inc.

Application

ANDA090182

Marketing category

ANDA

Marketing start

2011-09-08

Marketing end

0000-00-00

Substance

CETIRIZINE HYDROCHLORIDE

Active strength

1 mg/mL

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record