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Cetirizine Hydrochloride

NDC 76162-009 · HUMAN OTC DRUG · TABLET, ORALLY DISINTEGRATING

Labeler / ManufacturerTOPCO ASSOCIATES LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA213557
Dosage form / routeTABLET, ORALLY DISINTEGRATING · ORAL
Active ingredientsCETIRIZINE HYDROCHLORIDE (10 mg/1)
Marketing started20240606
Package count1

External sources

Source: openFDA. Public-domain (CC0).