Cetirizine Hydrochloride

Product NDC

70518-0777

11-digit product format

705180777

Labeler code

70518

Product ID

70518-0777_5b36f2ed-afac-2c3c-e053-2991aa0abb15

Type

HUMAN OTC DRUG

Nonproprietary name

Cetirizine Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA077946

Marketing category

ANDA

Marketing start

2017-10-10

Marketing end

0000-00-00

Substance

CETIRIZINE HYDROCHLORIDE

Active strength

5 mg/1

NDC exclude flag

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record