Prednisolone Sodium Phosphate 00121-0759
Product NDC
00121-0759- Manufacturer
- Pai Holdings, Llc Dba Pai Pharma
- Dosage Form
- Solution
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 25, 2005
- Listing Expires
- December 31, 2026
- Application
- ANDA076913
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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 (0121-0759-08)