Prednisolone Sodium Phosphate 17856-8815
Product NDC
17856-8815- 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(1)
50 CUP, UNIT-DOSE in 1 CASE (17856-8815-1) / 5 mL in 1 CUP, UNIT-DOSE