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Cetirizine Hydrochloride and Pseudoephedrine Hydrochloride

NDC 58602-703 · HUMAN OTC DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerAurohealth LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA212409
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsCETIRIZINE HYDROCHLORIDE (5 mg/1)
PSEUDOEPHEDRINE HYDROCHLORIDE (120 mg/1)
Marketing started20230308
Package count4

External sources

Source: openFDA. Public-domain (CC0).