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Sulfacetamide Sodium and Prednisolone Sodium Phosphate
Sulfacetamide Sodium and Prednisolone Sodium Phosphate - 21695-186-05 - (sulfacetamide sodium and prednisolone sodium phosphate)
Drug Information of Sulfacetamide Sodium and Prednisolone Sodium Phosphate
| Product NDC: | 21695-186 |
| Proprietary Name: | Sulfacetamide Sodium and Prednisolone Sodium Phosphate |
| Non Proprietary Name: | sulfacetamide sodium and prednisolone sodium phosphate |
| Active Ingredient(s): | 2.5; 100 mg/mL; mg/mL & nbsp; sulfacetamide sodium and prednisolone sodium phosphate |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sulfacetamide Sodium and Prednisolone Sodium Phosphate
| Product NDC: | 21695-186 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074449 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19951229 |
Package Information of Sulfacetamide Sodium and Prednisolone Sodium Phosphate
| Package NDC: | 21695-186-05 |
| Package Description: | 5 mL in 1 BOTTLE (21695-186-05) |
NDC Information of Sulfacetamide Sodium and Prednisolone Sodium Phosphate
| NDC Code | 21695-186-05 |
| Proprietary Name | Sulfacetamide Sodium and Prednisolone Sodium Phosphate |
| Package Description | 5 mL in 1 BOTTLE (21695-186-05) |
| Product NDC | 21695-186 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | sulfacetamide sodium and prednisolone sodium phosphate |
| Dosage Form Name | SOLUTION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 19951229 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | PREDNISOLONE SODIUM PHOSPHATE; SULFACETAMIDE SODIUM |
| Strength Number | 2.5; 100 |
| Strength Unit | mg/mL; mg/mL |
| Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
