FDA NDC Directory · JSON-LD · Markdown

Prednisolone Sodium Phosphate

NDC 0121-0759 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerPAI Holdings, LLC dba PAI Pharma
Marketing categoryAbbreviated NDA (generic) · App ANDA076913
Dosage form / routeSOLUTION · ORAL
Active ingredientsPREDNISOLONE SODIUM PHOSPHATE (15 mg/5mL)
Marketing started20050425
Package count1

External sources

Source: openFDA. Public-domain (CC0).