| Product NDC: | 45802-950 |
| Proprietary Name: | Perrigo Sodium Sulfacetamide and Sulfur |
| Non Proprietary Name: | Sodium Sulfacetamide and Sulfur |
| Active Ingredient(s): | & nbsp; Sodium Sulfacetamide and Sulfur |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 45802-950 |
| Labeler Name: | Perrigo New York Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20080820 |
| Package NDC: | 45802-950-01 |
| Package Description: | 1 KIT in 1 CARTON (45802-950-01) * 22.9 g in 1 BOTTLE * 2.1 g in 1 VIAL |
| NDC Code | 45802-950-01 |
| Proprietary Name | Perrigo Sodium Sulfacetamide and Sulfur |
| Package Description | 1 KIT in 1 CARTON (45802-950-01) * 22.9 g in 1 BOTTLE * 2.1 g in 1 VIAL |
| Product NDC | 45802-950 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sodium Sulfacetamide and Sulfur |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20080820 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Perrigo New York Inc |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
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