Product NDC: | 42808-100 |
Proprietary Name: | SODIUM SULFACETAMIDE |
Non Proprietary Name: | SODIUM SULFACETAMIDE |
Active Ingredient(s): | 100 mg/mL & nbsp; SODIUM SULFACETAMIDE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 42808-100 |
Labeler Name: | Exact-Rx, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20110801 |
Package NDC: | 42808-100-12 |
Package Description: | 354.8 mL in 1 BOTTLE (42808-100-12) |
NDC Code | 42808-100-12 |
Proprietary Name | SODIUM SULFACETAMIDE |
Package Description | 354.8 mL in 1 BOTTLE (42808-100-12) |
Product NDC | 42808-100 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | SODIUM SULFACETAMIDE |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20110801 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Exact-Rx, Inc. |
Substance Name | SULFACETAMIDE SODIUM |
Strength Number | 100 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |