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Levocetirizine Dihydrochloride

NDC 69230-321 · HUMAN OTC DRUG · TABLET, FILM COATED

Labeler / ManufacturerCamber Consumer Care Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA213513
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLEVOCETIRIZINE DIHYDROCHLORIDE (5 mg/1)
Marketing started20201028
Package count6

External sources

Source: openFDA. Public-domain (CC0).