Cetirizine Hydrochloride (Allergy)

Product NDC
50090-6168
Type
HUMAN OTC DRUG
Nonproprietary name
Cetirizine Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA090760
Marketing category
ANDA
Substance
CETIRIZINE HYDROCHLORIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-6168-130 TABLET in 1 BOTTLE (50090-6168-1) 2022-10-26NoHistorical
50090-6168-390 TABLET in 1 BOTTLE (50090-6168-3) 2023-08-02NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
158d3bcc-6a7f-4ee7-b181-be3fd6f94f8dA-S Medication Solutions2026-01-29Human OTC Drug Label4