| NDC Code | 53002-8690-2 |
|---|
| Package Description | 10 mL in 1 BOTTLE, DROPPER (53002-8690-2) |
|---|
| Product NDC | 53002-8690 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Sulfacetamide Sodium And Prednisolone Sodium Phosphate |
|---|
| Non-Proprietary Name | Sulfacetamide Sodium And Prednisolone Sodium Phosphate |
|---|
| Dosage Form | SOLUTION/ DROPS |
|---|
| Usage | OPHTHALMIC |
|---|
| Start Marketing Date | 19951229 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA074449 |
|---|
| Manufacturer | RPK Pharmaceuticals, Inc. |
|---|
| Substance Name | PREDNISOLONE SODIUM PHOSPHATE; SULFACETAMIDE SODIUM |
|---|
| Strength | 2.3; 100 |
|---|
| Strength Unit | mg/mL; mg/mL |
|---|
| Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Sulfonamide Antibacterial [EPC], Sulfonamides [CS] |
|---|