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levocetirizine dihydrochloride

NDC 69842-761 · HUMAN OTC DRUG · TABLET, COATED

Labeler / ManufacturerCVS PHARMACY
Marketing categoryAbbreviated NDA (generic) · App ANDA210375
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsLEVOCETIRIZINE DIHYDROCHLORIDE (5 mg/1)
Marketing started20180415
Package count4

External sources

Source: openFDA. Public-domain (CC0).