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Fexofenadine HCl and Pseudoephedrine HCI

NDC 43598-823 · HUMAN OTC DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerDr. Reddy's Laboratories Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA076667
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsFEXOFENADINE HYDROCHLORIDE (60 mg/1)
PSEUDOEPHEDRINE HYDROCHLORIDE (120 mg/1)
Marketing started20190718
Package count3

External sources

Source: openFDA. Public-domain (CC0).