| NDC Code | 24208-317-10 |
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| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (24208-317-10) / 10 mL in 1 BOTTLE, DROPPER |
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| Product NDC | 24208-317 |
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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/ DROPS |
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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 | Bausch & Lomb Incoporated |
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| Substance Name | PREDNISOLONE SODIUM PHOSPHATE; SULFACETAMIDE SODIUM |
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| Strength | 2.3; 100 |
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| Strength Unit | mg/mL; mg/mL |
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| Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Sulfonamide Antibacterial [EPC], Sulfonamides [CS] |
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