FDA NDC Directory · JSON-LD · Markdown

PrednisoLONE Sodium Phosphate

NDC 0121-1100 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerPAI Holdings, LLC dba PAI Pharma
Marketing categoryNew Drug Application (innovator) · App NDA019157
Dosage form / routeSOLUTION · ORAL
Active ingredientsPREDNISOLONE SODIUM PHOSPHATE (5 mg/5mL)
Marketing started20260626
Package count1

External sources

Source: openFDA. Public-domain (CC0).