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cetirizine hydrochloride

NDC 70677-1007 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameCetirizine Hydrochloride Tablets
Labeler / ManufacturerStrategic Sourcing Services LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA078343
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCETIRIZINE HYDROCHLORIDE (10 mg/1)
Marketing started20220512
Marketing ended20270228
Package count4

External sources

Source: openFDA. Public-domain (CC0).