Cetirizine Hydrochloride

Product NDC

70518-1989

11-digit product format

705181989

Labeler code

70518

Product ID

70518-1989_970b83dc-b17b-9f5d-e053-2a95a90a3231

Type

HUMAN OTC DRUG

Nonproprietary name

Cetirizine Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA078317

Marketing category

ANDA

Marketing start

2019-03-27

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