FDA NDC Directory · JSON-LD · Markdown

Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride

NDC 79903-108 · HUMAN OTC DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerWal-mart Stores, Inc.
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 count2

External sources

Source: openFDA. Public-domain (CC0).