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