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Childrens Cetirizine Hydrochloride

NDC 51672-2147 · HUMAN OTC DRUG · SOLUTION

Generic nameCetirizine Hydrochloride
Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090182
Dosage form / routeSOLUTION · ORAL
Active ingredientsCETIRIZINE HYDROCHLORIDE (1 mg/mL)
Marketing started20250320
Package count2

External sources

Source: openFDA. Public-domain (CC0).