FDA NDC Directory · JSON-LD · Markdown

Fexofenadine HCl and Pseudoephedrine HCI

NDC 0363-1606 · HUMAN OTC DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerWalgreens Company
Marketing categoryAbbreviated NDA (generic) · App ANDA076667
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (60 mg/1)
PSEUDOEPHEDRINE HYDROCHLORIDE (120 mg/1)
Marketing started20190916
Package count2

External sources

Source: openFDA. Public-domain (CC0).