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Cetirizine hydrochloride and Pseudoephedrine hydrochloride

NDC 45802-147 · HUMAN OTC DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Generic nameCetirizine hydrochloride, Pseudoephedrine hydrochloride
Labeler / ManufacturerPadagis Israel Pharmaceuticals Ltd
Marketing categoryAbbreviated NDA (generic) · App ANDA210719
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsCETIRIZINE HYDROCHLORIDE (5 mg/1)
PSEUDOEPHEDRINE HYDROCHLORIDE (120 mg/1)
Marketing started20200331
Package count2

External sources

Source: openFDA. Public-domain (CC0).