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Cetirizine Hydrochloride Tablets,10 mg

NDC 51655-842 · HUMAN OTC DRUG · TABLET

Generic nameCetirizine Hydrochloride
Labeler / ManufacturerNorthwind Health Company, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA078933
Dosage form / routeTABLET · ORAL
Active ingredientsCETIRIZINE HYDROCHLORIDE (10 mg/1)
Marketing started20230207
Package count4

External sources

Source: openFDA. Public-domain (CC0).