Cetirizine Hydrochloride

Product NDC

70518-0910

11-digit product format

705180910

Labeler code

70518

Product ID

70518-0910_8f096f20-b5a0-4b6c-e053-2a95a90a5cc4

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

2017-12-14

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