Prednisolone Sodium Phosphate 68999-0330
Product NDC
68999-0330- Manufacturer
- Chartwell Governmental & Specialty Rx, Llc.
- Dosage Form
- Solution
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 25, 2004
- Listing Expires
- December 31, 2026
- Application
- ANDA075988
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Prednisolone Sodium Phosphate | 5 mg/5mL |
Drug Class
Corticosteroid Hormone Receptor Agonists [MoA]Corticosteroid [EPC]
Packaging Options(1)
2 TRAY in 1 BOX (68999-330-24) / 10 CUP in 1 TRAY / 5 mL in 1 CUP (68999-330-05)