7 select all day allergy

Product NDC

10202-458

11-digit product format

102020458

Labeler code

10202

Product ID

10202-458_09510cfd-8077-4094-8d8d-b055a5f24c14

Type

HUMAN OTC DRUG

Nonproprietary name

Cetirizine Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

7-Eleven

Application

ANDA078336

Marketing category

ANDA

Marketing start

2014-04-29

Marketing end

2021-01-31

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