Cetirizine Hydrochloride (Allergy)

Product NDC
50090-6950
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
50090-6950-030 TABLET in 1 BOTTLE (50090-6950-0) 2023-12-19NoHistorical
50090-6950-190 TABLET in 1 BOTTLE (50090-6950-1) 2026-01-28NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
ae02b16b-77dc-4bd6-8c07-e734fb448492A-S Medication Solutions2026-01-29Human OTC Drug Label4