Cetirizine Hydrochloride

Product NDC

60687-165

11-digit product format

606870165

Labeler code

60687

Product ID

60687-165_8177534e-7394-50b9-e053-2991aa0a52b4

Type

HUMAN OTC DRUG

Nonproprietary name

Cetirizine Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

American Health Packaging

Application

ANDA078317

Marketing category

ANDA

Marketing start

2015-06-17

Marketing end

2020-04-30

Substance

CETIRIZINE HYDROCHLORIDE

Active strength

10 mg/1

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record