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Cetirizine Hydrochloride

NDC 0378-3637 · HUMAN OTC DRUG · TABLET, FILM COATED

Generic namecetirizine hydrochloride
Labeler / ManufacturerMylan Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076677
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCETIRIZINE HYDROCHLORIDE (10 mg/1)
Marketing started20071227
Package count2

External sources

Source: openFDA. Public-domain (CC0).