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Cetirizine Hydrochloride

NDC 45802-626 · HUMAN PRESCRIPTION DRUG · SOLUTION

Generic nameCetirizine hydrochloride
Labeler / ManufacturerPadagis Israel Pharmaceuticals Ltd
Marketing categoryAbbreviated NDA (generic) · App ANDA078398
Dosage form / routeSOLUTION · ORAL
Active ingredientsCETIRIZINE HYDROCHLORIDE (1 mg/mL)
Marketing started20080724
Package count1

External sources

Source: openFDA. Public-domain (CC0).