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levocetirizine dihydrochloride

NDC 68788-7934 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPreferred Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA203646
Dosage form / routeTABLET · ORAL
Active ingredientsLEVOCETIRIZINE DIHYDROCHLORIDE (5 mg/1)
Marketing started20210615
Package count4

External sources

Source: openFDA. Public-domain (CC0).