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Clenia
Clenia - 0245-0169-01 - (sulfacetamide sodium and sulfur)
Drug Information of Clenia
| Product NDC: | 0245-0169 |
| Proprietary Name: | Clenia |
| Non Proprietary Name: | sulfacetamide sodium and sulfur |
| Active Ingredient(s): | 100; 50 mg/g; mg/g & nbsp; sulfacetamide sodium and sulfur |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Clenia
| Product NDC: | 0245-0169 |
| Labeler Name: | Upsher-Smith Laboratories, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20090901 |
Package Information of Clenia
| Package NDC: | 0245-0169-01 |
| Package Description: | 1 TUBE in 1 CARTON (0245-0169-01) > 28 g in 1 TUBE |
NDC Information of Clenia
| NDC Code | 0245-0169-01 |
| Proprietary Name | Clenia |
| Package Description | 1 TUBE in 1 CARTON (0245-0169-01) > 28 g in 1 TUBE |
| Product NDC | 0245-0169 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | sulfacetamide sodium and sulfur |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20090901 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Upsher-Smith Laboratories, Inc |
| Substance Name | SULFACETAMIDE SODIUM; SULFUR |
| Strength Number | 100; 50 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |
