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Cetirizine Hydrochloride

NDC 51660-939 · HUMAN OTC DRUG · TABLET

Labeler / ManufacturerOhm Laboratories Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077498
Dosage form / routeTABLET · ORAL
Active ingredientsCETIRIZINE HYDROCHLORIDE (10 mg/1)
Marketing started20071227
Package count6

External sources

Source: openFDA. Public-domain (CC0).