FDA NDC Directory · JSON-LD · Markdown

Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride

NDC 51316-015 · HUMAN OTC DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerCVS Health Corp
Marketing categoryAbbreviated NDA (generic) · App ANDA215434
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (60 mg/1)
PSEUDOEPHEDRINE HYDROCHLORIDE (120 mg/1)
Marketing started20220603
Package count2

External sources

Source: openFDA. Public-domain (CC0).