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CABINET Allergy Relief

NDC 68210-0119 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameCetirizine Hydrochloride
Labeler / ManufacturerSpirit Pharmaceutical LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA209274
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCETIRIZINE HYDROCHLORIDE (10 mg/1)
Marketing started20191025
Package count3

External sources

Source: openFDA. Public-domain (CC0).