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Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride

NDC 58602-807 · HUMAN OTC DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerAurohealth LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA209116
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (60 mg/1)
PSEUDOEPHEDRINE HYDROCHLORIDE (120 mg/1)
Marketing started20171030
Package count3

External sources

Source: openFDA. Public-domain (CC0).