FDA NDC Directory · JSON-LD · Markdown

Prednisolone Sodium Phosphate

NDC 42799-813 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerEdenbridge Pharmaceuticals LLC.
Marketing categoryAbbreviated NDA (generic) · App ANDA203559
Dosage form / routeSOLUTION · ORAL
Active ingredientsPREDNISOLONE SODIUM PHOSPHATE (20 mg/5mL)
Marketing started20111111
Package count1

External sources

Source: openFDA. Public-domain (CC0).