Cetirizine Hydrochloride

Product NDC

68788-9734

11-digit product format

687889734

Labeler code

68788

Product ID

68788-9734_2135ae86-f419-47db-8036-dfa889a59218

Type

HUMAN OTC DRUG

Nonproprietary name

Cetirizine Hydrochloride

Dosage form

SOLUTION

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA090182

Marketing category

ANDA

Marketing start

2012-10-22

Marketing end

0000-00-00

Substance

CETIRIZINE HYDROCHLORIDE

Active strength

1 mg/mL

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record