FDA
Prednisolone Sodium Phosphate
The FDA lists this product in 36 strengths and forms.
Composition
- Active ingredients
- PREDNISOLONE SODIUM PHOSPHATE EQ 0.9% PHOSPHATE
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- PREDNISOLONE SODIUM PHOSPHATE EQ 0.11% PHOSPHATE · Solution/dropsANDA081043-001 · Discontinued
- PREDNISOLONE SODIUM PHOSPHATE EQ 5MG BASE/5ML · SolutionANDA075099-001 · Discontinued
- PREDNISOLONE SODIUM PHOSPHATE EQ 5MG BASE/5ML · SolutionANDA075183-001 · Discontinued
- PREDNISOLONE SODIUM PHOSPHATE EQ 5MG BASE/5ML · SolutionANDA076123-001 · Discontinued
- PREDNISOLONE SODIUM PHOSPHATE EQ 15MG BASE/5ML · SolutionANDA076913-001 · Prescription
- PREDNISOLONE SODIUM PHOSPHATE EQ 0.9% PHOSPHATE · Solution/dropsANDA084169-001 · Discontinued
- PREDNISOLONE SODIUM PHOSPHATE EQ 15MG BASE/5ML · SolutionANDA203559-003 · Prescription
- PREDNISOLONE SODIUM PHOSPHATE EQ 10MG BASE/5ML · SolutionANDA203559-001 · Prescription
- PREDNISOLONE SODIUM PHOSPHATE EQ 25MG BASE/5ML · SolutionANDA203559-004 · Prescription
- PREDNISOLONE SODIUM PHOSPHATE EQ 20MG BASE/5ML · Solution
At a glance
- Brand name
- Prednisolone Sodium Phosphate
- Route
- Eye
- Dosage form
- Solution/drops
- Applicant
- Epic Pharma LLC
- Status
- Discontinued
- FDA approval
- 21 Aug 1974
- Application
- ANDA083358-002