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Levocetirizine Dihydrochloride

NDC 43063-479 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090199
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLEVOCETIRIZINE DIHYDROCHLORIDE (5 mg/1)
Marketing started20110906
Package count1

External sources

Source: openFDA. Public-domain (CC0).