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SODIUM SULFACETAMIDE, SULFUR
SODIUM SULFACETAMIDE, SULFUR - 42808-110-12 - (SODIUM SULFACETAMIDE, SULFUR)
Drug Information of SODIUM SULFACETAMIDE, SULFUR
| Product NDC: | 42808-110 |
| Proprietary Name: | SODIUM SULFACETAMIDE, SULFUR |
| Non Proprietary Name: | SODIUM SULFACETAMIDE, SULFUR |
| Active Ingredient(s): | 100; 50 mg/g; mg/g & nbsp; SODIUM SULFACETAMIDE, SULFUR |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SODIUM SULFACETAMIDE, SULFUR
| Product NDC: | 42808-110 |
| Labeler Name: | Exact-Rx, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110801 |
Package Information of SODIUM SULFACETAMIDE, SULFUR
| Package NDC: | 42808-110-12 |
| Package Description: | 2 TUBE in 1 CARTON (42808-110-12) > 170 g in 1 TUBE |
NDC Information of SODIUM SULFACETAMIDE, SULFUR
| NDC Code | 42808-110-12 |
| Proprietary Name | SODIUM SULFACETAMIDE, SULFUR |
| Package Description | 2 TUBE in 1 CARTON (42808-110-12) > 170 g in 1 TUBE |
| Product NDC | 42808-110 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SODIUM SULFACETAMIDE, SULFUR |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20110801 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Exact-Rx, Inc. |
| Substance Name | SULFACETAMIDE SODIUM; SULFUR |
| Strength Number | 100; 50 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |
