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SODIUM SULFACETAMIDE and SULFUR
SODIUM SULFACETAMIDE and SULFUR - 49908-173-80 - (SODIUM SULFACETAMIDE and SULFUR)
Drug Information of SODIUM SULFACETAMIDE and SULFUR
| Product NDC: | 49908-173 |
| Proprietary Name: | SODIUM SULFACETAMIDE and SULFUR |
| Non Proprietary Name: | SODIUM SULFACETAMIDE and SULFUR |
| Active Ingredient(s): | 90; 45 mg/g; mg/g & nbsp; SODIUM SULFACETAMIDE and SULFUR |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of SODIUM SULFACETAMIDE and SULFUR
| Product NDC: | 49908-173 |
| Labeler Name: | Rochester Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110804 |
Package Information of SODIUM SULFACETAMIDE and SULFUR
| Package NDC: | 49908-173-80 |
| Package Description: | 1 BOTTLE, PUMP in 1 CARTON (49908-173-80) > 454 g in 1 BOTTLE, PUMP |
NDC Information of SODIUM SULFACETAMIDE and SULFUR
| NDC Code | 49908-173-80 |
| Proprietary Name | SODIUM SULFACETAMIDE and SULFUR |
| Package Description | 1 BOTTLE, PUMP in 1 CARTON (49908-173-80) > 454 g in 1 BOTTLE, PUMP |
| Product NDC | 49908-173 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SODIUM SULFACETAMIDE and SULFUR |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110804 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Rochester Pharmaceuticals |
| Substance Name | SULFACETAMIDE SODIUM; SULFUR |
| Strength Number | 90; 45 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |
