Cetirizine

Product NDC

70518-2335

11-digit product format

705182335

Labeler code

70518

Product ID

70518-2335_93f719e2-d373-0b49-e053-2a95a90ab6af

Type

HUMAN OTC DRUG

Nonproprietary name

Cetirizine Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA078336

Marketing category

ANDA

Marketing start

2019-10-02

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