FDA NDC Directory · JSON-LD · Markdown

Prednisolone Sodium Phosphate

NDC 0121-0777 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerPAI Holdings, LLC dba PAI Pharma
Marketing categoryAbbreviated NDA (generic) · App ANDA078988
Dosage form / routeSOLUTION · ORAL
Active ingredientsPREDNISOLONE SODIUM PHOSPHATE (20 mg/5mL)
Marketing started20170131
Package count1

External sources

Source: openFDA. Public-domain (CC0).