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Cetirizine

NDC 0904-6717 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic nameCetirizine Hydrochloride
Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA078336
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCETIRIZINE HYDROCHLORIDE (10 mg/1)
Marketing started20180629
Package count8

External sources

Source: openFDA. Public-domain (CC0).