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Cetirizine Hydrochloride

NDC 71205-093 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA077829
Dosage form / routeTABLET · ORAL
Active ingredientsCETIRIZINE HYDROCHLORIDE (5 mg/1)
Marketing started20091001
Package count4

External sources

Source: openFDA. Public-domain (CC0).