FDA NDC Directory · JSON-LD · Markdown

Prednisolone Sodium Phosphate

NDC 17856-0815 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerATLANTIC BIOLOGICALS CORP.
Marketing categoryAbbreviated NDA (generic) · App ANDA203559
Dosage form / routeSOLUTION · ORAL
Active ingredientsPREDNISOLONE SODIUM PHOSPHATE (15 mg/5mL)
Marketing started20231009
Package count3

External sources

Source: openFDA. Public-domain (CC0).