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Sulfacetamide Sodium
Sulfacetamide Sodium - 51672-1346-8 - (Sulfacetamide Sodium)
Drug Information of Sulfacetamide Sodium
| Product NDC: | 51672-1346 |
| Proprietary Name: | Sulfacetamide Sodium |
| Non Proprietary Name: | Sulfacetamide Sodium |
| Active Ingredient(s): | 100 mg/mL & nbsp; Sulfacetamide Sodium |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sulfacetamide Sodium
| Product NDC: | 51672-1346 |
| Labeler Name: | Taro Pharmaceuticals U.S.A., Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078668 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090520 |
Package Information of Sulfacetamide Sodium
| Package NDC: | 51672-1346-8 |
| Package Description: | 1 BOTTLE in 1 CARTON (51672-1346-8) > 118 mL in 1 BOTTLE |
NDC Information of Sulfacetamide Sodium
| NDC Code | 51672-1346-8 |
| Proprietary Name | Sulfacetamide Sodium |
| Package Description | 1 BOTTLE in 1 CARTON (51672-1346-8) > 118 mL in 1 BOTTLE |
| Product NDC | 51672-1346 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sulfacetamide Sodium |
| Dosage Form Name | SUSPENSION |
| Route Name | TOPICAL |
| Start Marketing Date | 20090520 |
| Marketing Category Name | ANDA |
| Labeler Name | Taro Pharmaceuticals U.S.A., Inc. |
| Substance Name | SULFACETAMIDE SODIUM |
| Strength Number | 100 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |
