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Fexofenadine HCl and Pseudoephedrine HCl

NDC 43598-892 · HUMAN OTC DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerDr.Reddy's Laboratories Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA079043
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (180 mg/1)
PSEUDOEPHEDRINE HYDROCHLORIDE (240 mg/1)
Marketing started20220517
Marketing ended20260831
Package count2

External sources

Source: openFDA. Public-domain (CC0).