FDA NDC Directory · JSON-LD · Markdown

Cetirizine Hydrochloride

NDC 10135-762 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerMarlex Pharmaceuticals, Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA077498
Dosage form / routeTABLET · ORAL
Active ingredientsCETIRIZINE HYDROCHLORIDE (10 mg/1)
Marketing started20221001
Package count5

External sources

Source: openFDA. Public-domain (CC0).