FDA NDC Directory · JSON-LD · Markdown

Orapred ODT

NDC 59212-700 · HUMAN PRESCRIPTION DRUG · TABLET, ORALLY DISINTEGRATING

Generic nameprednisolone sodium phosphate
Labeler / ManufacturerAdvanz Pharma (US) Corp.
Marketing categoryNew Drug Application (innovator) · App NDA021959
Dosage form / routeTABLET, ORALLY DISINTEGRATING · ORAL
Active ingredientsPREDNISOLONE SODIUM PHOSPHATE (10 mg/1)
Marketing started20060601
Package count1

External sources

Source: openFDA. Public-domain (CC0).