FDA NDC Directory · JSON-LD · Markdown

Cetirizine Hydrochloride

NDC 81469-352 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerFirst Nation Group, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA076047
Dosage form / routeTABLET · ORAL
Active ingredientsCETIRIZINE HYDROCHLORIDE (5 mg/1)
Marketing started20261002
Package count1

External sources

Source: openFDA. Public-domain (CC0).