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Cetirizine Hydrochloride

NDC 65162-045 · HUMAN OTC DRUG · TABLET

Generic nameCetirizine
Labeler / ManufacturerAmneal Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA078780
Dosage form / routeTABLET · ORAL
Active ingredientsCETIRIZINE HYDROCHLORIDE (5 mg/1)
Marketing started20100121
Package count2

External sources

Source: openFDA. Public-domain (CC0).