allergy relief

Product NDC

41250-721

11-digit product format

412500721

Labeler code

41250

Product ID

41250-721_f89f2fdc-cf41-4f24-8024-3a2d277a34a7

Type

HUMAN OTC DRUG

Nonproprietary name

Cetirizine Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Meijer, Inc.

Application

ANDA078336

Marketing category

ANDA

Marketing start

2017-07-12

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