FDA NDC Directory · JSON-LD · Markdown

Allergy Relief

NDC 46122-531 · HUMAN OTC DRUG · TABLET, COATED

Generic namelevocetirizine dihydrochloride
Labeler / ManufacturerAMERISOURCEBERGEN DRUG CORPORATION
Marketing categoryAbbreviated NDA (generic) · App ANDA210375
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsLEVOCETIRIZINE DIHYDROCHLORIDE (5 mg/1)
Marketing started20180420
Package count2

External sources

Source: openFDA. Public-domain (CC0).