Prednisolone Sodium Phosphate 17856-0815
Product NDC
17856-0815- Manufacturer
- Atlantic Biologicals Corp.
- Dosage Form
- Solution
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 9, 2023
- Listing Expires
- December 31, 2026
- Application
- ANDA203559
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Prednisolone Sodium Phosphate | 15 mg/5mL |
Drug Class
Corticosteroid Hormone Receptor Agonists [MoA]Corticosteroid [EPC]
Packaging Options(3)
72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0815-1) / 5 mL in 1 CUP, UNIT-DOSE
72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0815-2) / 10 mL in 1 CUP, UNIT-DOSE
48 SYRINGE in 1 BOX, UNIT-DOSE (17856-0815-3) / 5 mL in 1 SYRINGE