FDA NDC Directory · JSON-LD · Markdown

Cetirizine Hydrochloride Tablets, 10 mg

NDC 25000-220 · HUMAN OTC DRUG · TABLET

Generic nameCetirizine Hydrochloride
Labeler / ManufacturerMARKSANS PHARMA LIMITED
Marketing categoryAbbreviated NDA (generic) · App ANDA078933
Dosage form / routeTABLET · ORAL
Active ingredientsCETIRIZINE HYDROCHLORIDE (10 mg/1)
Marketing started20220113
Package count5

External sources

Source: openFDA. Public-domain (CC0).