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Levocetirizine Dihydrochloride

NDC 31722-551 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerCamber Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA091264
Dosage form / routeTABLET · ORAL
Active ingredientsLEVOCETIRIZINE DIHYDROCHLORIDE (5 mg/1)
Marketing started20120629
Package count5

External sources

Source: openFDA. Public-domain (CC0).