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 | |
Pharmaceutical Classes |