| Product NDC: | 61314-701 |
| Proprietary Name: | Sulfacetamide Sodium |
| Non Proprietary Name: | Sulfacetamide Sodium |
| Active Ingredient(s): | 100 mg/mL & nbsp; Sulfacetamide Sodium |
| Administration Route(s): | OPHTHALMIC |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 61314-701 |
| Labeler Name: | Falcon Pharmaceuticals, Ltd. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA089560 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20030325 |
| Package NDC: | 61314-701-01 |
| Package Description: | 15 mL in 1 BOTTLE, PLASTIC (61314-701-01) |
| NDC Code | 61314-701-01 |
| Proprietary Name | Sulfacetamide Sodium |
| Package Description | 15 mL in 1 BOTTLE, PLASTIC (61314-701-01) |
| Product NDC | 61314-701 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sulfacetamide Sodium |
| Dosage Form Name | SOLUTION |
| Route Name | OPHTHALMIC |
| Start Marketing Date | 20030325 |
| Marketing Category Name | ANDA |
| Labeler Name | Falcon Pharmaceuticals, Ltd. |
| Substance Name | SULFACETAMIDE SODIUM |
| Strength Number | 100 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |