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NDC 46122-626 · HUMAN OTC DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Generic nameCetirizine hydrochloride, Pseudoephedrine hydrochloride
Labeler / ManufacturerAmerisource Bergen
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 started20200330
Package count1

External sources

Source: openFDA. Public-domain (CC0).