All Day Allergy Relief

Product NDC

55910-220

11-digit product format

559100220

Labeler code

55910

Product ID

55910-220_7f2c16bd-b13a-4b7f-9772-5e963daf416d

Type

HUMAN OTC DRUG

Nonproprietary name

Cetirizine HCl

Dosage form

TABLET

Route

ORAL

Labeler

Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)

Application

ANDA078427

Marketing category

ANDA

Marketing start

2012-10-19

Marketing end

0000-00-00

Substance

CETIRIZINE HYDROCHLORIDE

Active strength

10 mg/1

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record