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Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride

NDC 70677-1010 · HUMAN OTC DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerStrategic Sourcing Services, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA215434
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (60 mg/1)
PSEUDOEPHEDRINE HYDROCHLORIDE (120 mg/1)
Marketing started20220331
Package count1

External sources

Source: openFDA. Public-domain (CC0).