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Cefpodoxime Proxetil

NDC 67877-559 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAscend Laboratories, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA210568
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsCEFPODOXIME PROXETIL (100 mg/1)
Marketing started20220519
Package count3

External sources

Source: openFDA. Public-domain (CC0).