FDA NDC Directory · JSON-LD · Markdown

Cetirizine Hydrochloride

NDC 16571-401 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerRising Pharma Holdings, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077829
Dosage form / routeTABLET · ORAL
Active ingredientsCETIRIZINE HYDROCHLORIDE (5 mg/1)
Marketing started20091001
Package count1

External sources

Source: openFDA. Public-domain (CC0).