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Cetirizine hydrochloride

NDC 80513-731 · HUMAN OTC DRUG · TABLET, COATED

Labeler / ManufacturerAdvanced Rx LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA209274
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsCETIRIZINE HYDROCHLORIDE (10 mg/1)
Marketing started20250501
Package count2

External sources

Source: openFDA. Public-domain (CC0).