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cetirizine hydrochloride

NDC 68788-4072 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameCetirizine Hydrochloride
Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078336
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCETIRIZINE HYDROCHLORIDE (10 mg/1)
Marketing started20260127
Package count3

External sources

Source: openFDA. Public-domain (CC0).