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Cetirizine Hydrochloride

NDC 53943-519 · HUMAN OTC DRUG · TABLET, FILM COATED

Labeler / ManufacturerDiscount Drug Mart, Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA078343
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCETIRIZINE HYDROCHLORIDE (10 mg/1)
Marketing started20200120
Package count2

External sources

Source: openFDA. Public-domain (CC0).