NDC Code | 21695-186-05 |
Package Description | 5 mL in 1 BOTTLE (21695-186-05) |
Product NDC | 21695-186 |
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 |
Usage | OPHTHALMIC |
Start Marketing Date | 19951229 |
Marketing Category Name | ANDA |
Application Number | ANDA074449 |
Manufacturer | Rebel Distributors Corp |
Substance Name | SULFACETAMIDE SODIUM; PREDNISOLONE SODIUM PHOSPHATE |
Strength | 100; 2.5 |
Strength Unit | mg/mL; mg/mL |
Pharmacy Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [CS],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |