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Klaron
Klaron - 0066-7500-04 - (sulfacetamide sodium)
Drug Information of Klaron
| Product NDC: | 0066-7500 |
| Proprietary Name: | Klaron |
| Non Proprietary Name: | sulfacetamide sodium |
| Active Ingredient(s): | 10 mg/mL & nbsp; sulfacetamide sodium |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Klaron
| Product NDC: | 0066-7500 |
| Labeler Name: | Dermik Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019931 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19961223 |
Package Information of Klaron
| Package NDC: | 0066-7500-04 |
| Package Description: | 118 mL in 1 BOTTLE, PLASTIC (0066-7500-04) |
NDC Information of Klaron
| NDC Code | 0066-7500-04 |
| Proprietary Name | Klaron |
| Package Description | 118 mL in 1 BOTTLE, PLASTIC (0066-7500-04) |
| Product NDC | 0066-7500 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | sulfacetamide sodium |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 19961223 |
| Marketing Category Name | NDA |
| Labeler Name | Dermik Laboratories |
| Substance Name | SULFACETAMIDE SODIUM |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |
