Cetirizine Hydrochloride

Product NDC

70518-0664

11-digit product format

705180664

Labeler code

70518

Product ID

70518-0664_7fafa231-0d91-0da7-e053-2991aa0ac004

Type

HUMAN OTC DRUG

Nonproprietary name

Cetirizine Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA077946

Marketing category

ANDA

Marketing start

2017-08-08

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