FDA NDC Directory · JSON-LD · Markdown

LEVOCETIRIZINE DIHYDROCHLORIDE

NDC 68462-346 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namelevocetirizine dihydrochloride
Labeler / ManufacturerGlenmark Pharmaceuticals Inc., USA
Marketing categoryAbbreviated NDA (generic) · App ANDA090385
Dosage form / routeTABLET · ORAL
Active ingredientsLEVOCETIRIZINE DIHYDROCHLORIDE (5 mg/1)
Marketing started20110225
Package count1

External sources

Source: openFDA. Public-domain (CC0).