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Cetirizine hydrochloride

NDC 69729-139 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerOPMX LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA209274
Dosage form / routeTABLET · ORAL
Active ingredientsCETIRIZINE HYDROCHLORIDE (10 mg/1)
Marketing started20200701
Package count1

External sources

Source: openFDA. Public-domain (CC0).