Cetirizine

Product NDC

60505-4322

11-digit product format

605054322

Labeler code

60505

Product ID

60505-4322_07dde544-9e21-904d-c2ec-70e7f60b0ad2

Type

HUMAN OTC DRUG

Nonproprietary name

Cetirizine

Dosage form

CAPSULE, LIQUID FILLED

Route

ORAL

Labeler

Apotex Corp.

Application

ANDA207235

Marketing category

ANDA

Marketing start

2017-07-07

Marketing end

0000-00-00

Substance

CETIRIZINE HYDROCHLORIDE

Active strength

10 mg/1

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record