FDA NDC Directory · JSON-LD · Markdown

Cefpodoxime Proxetil

NDC 70518-4676 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA210568
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCEFPODOXIME PROXETIL (200 mg/1)
Marketing started20260604
Package count1

External sources

Source: openFDA. Public-domain (CC0).