FDA NDC Directory · JSON-LD · Markdown

LEVOCETIRIZINE DIHYDROCHLORIDE

NDC 33342-200 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerMacleods Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA205564
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLEVOCETIRIZINE DIHYDROCHLORIDE (5 mg/1)
Marketing started20160111
Package count2

External sources

Source: openFDA. Public-domain (CC0).