Prednisolone Sodium Phosphate 24208-0715
Product NDC
24208-0715- Manufacturer
- Bausch & Lomb Incorporated
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Product Type
- Human Prescription Drug
- Marketing Start
- July 29, 1994
- Listing Expires
- December 31, 2026
- Application
- ANDA040070
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Prednisolone Sodium Phosphate | 10 mg/mL |
Drug Class
Corticosteroid Hormone Receptor Agonists [MoA]Corticosteroid [EPC]
Packaging Options(1)
1 BOTTLE, DROPPER in 1 CARTON (24208-715-10) / 10 mL in 1 BOTTLE, DROPPER