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Cetirizine Hydrochloride

NDC 47335-343 · HUMAN OTC DRUG · TABLET, CHEWABLE

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090142
Dosage form / routeTABLET, CHEWABLE · ORAL
Active ingredientsCETIRIZINE HYDROCHLORIDE (5 mg/1)
Marketing started20110909
Package count2

External sources

Source: openFDA. Public-domain (CC0).