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Cetirizine Hydrochloride (Allergy)

NDC 30142-172 · HUMAN OTC DRUG · TABLET

Generic nameCetirizine Hydrochloride
Labeler / ManufacturerKROGER COMPANY
Marketing categoryAbbreviated NDA (generic) · App ANDA090760
Dosage form / routeTABLET · ORAL
Active ingredientsCETIRIZINE HYDROCHLORIDE (10 mg/1)
Marketing started20210315
Package count2

External sources

Source: openFDA. Public-domain (CC0).