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Cetirizine Hydrochloride

NDC 55111-351 · HUMAN OTC DRUG · TABLET, FILM COATED

Labeler / ManufacturerDr.Reddy's Laboratories Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA078343
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCETIRIZINE HYDROCHLORIDE (10 mg/1)
Marketing started20080115
Package count8

External sources

Source: openFDA. Public-domain (CC0).