Sulfacetamide Sodium And Prednisolone Sodium Phosphate 68071-1650
Product NDC
68071-1650- Manufacturer
- Nucare Pharmaceuticals,inc.
- Dosage Form
- Solution/ Drops
- Route
- Ophthalmic
- Product Type
- Human Prescription Drug
- Marketing Start
- December 29, 1995
- Listing Expires
- December 31, 2026
- Application
- ANDA074449
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Prednisolone Sodium Phosphate | 2.3 mg/mL |
| Sulfacetamide Sodium | 100 mg/mL |
Drug Class
Corticosteroid Hormone Receptor Agonists [MoA]Corticosteroid [EPC]Sulfonamide Antibacterial [EPC]
Packaging Options(1)
5 mL in 1 BOX (68071-1650-5)
External Resources