Cetirizine Hydrochloride

Product NDC

68788-6905

11-digit product format

687886905

Labeler code

68788

Product ID

68788-6905_3d4f8a85-797b-404d-8e13-0e5556c222c9

Type

HUMAN OTC DRUG

Nonproprietary name

Cetirizine Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Preferred Pharmaceuticals Inc.

Application

ANDA077946

Marketing category

ANDA

Marketing start

2017-02-23

Marketing end

0000-00-00

Substance

CETIRIZINE HYDROCHLORIDE

Active strength

10 mg/1

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record