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Levocetirizine Dihydrochloride

NDC 42571-122 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namelevocetirizine Dihydrochloride
Labeler / ManufacturerMicro Labs Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA202046
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLEVOCETIRIZINE DIHYDROCHLORIDE (5 mg/1)
Marketing started20130930
Package count4

External sources

Source: openFDA. Public-domain (CC0).