Prednisolone Sodium Phosphate 69238-2122
Product NDC
69238-2122- Manufacturer
- Amneal Pharmaceuticals Ny Llc
- Dosage Form
- Solution
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 27, 2022
- Listing Expires
- December 31, 2026
- Application
- ANDA216715
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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)
237 mL in 1 BOTTLE (69238-2122-9)