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Sklice
Sklice - 49281-183-71 - (ivermectin)
Drug Information of Sklice
| Product NDC: | 49281-183 |
| Proprietary Name: | Sklice |
| Non Proprietary Name: | ivermectin |
| Active Ingredient(s): | .585 g/117g & nbsp; ivermectin |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sklice
| Product NDC: | 49281-183 |
| Labeler Name: | Sanofi Pasteur, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA202736 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20120709 |
Package Information of Sklice
| Package NDC: | 49281-183-71 |
| Package Description: | 1 TUBE in 1 BOX (49281-183-71) > 117 g in 1 TUBE |
NDC Information of Sklice
| NDC Code | 49281-183-71 |
| Proprietary Name | Sklice |
| Package Description | 1 TUBE in 1 BOX (49281-183-71) > 117 g in 1 TUBE |
| Product NDC | 49281-183 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ivermectin |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20120709 |
| Marketing Category Name | NDA |
| Labeler Name | Sanofi Pasteur, Inc |
| Substance Name | IVERMECTIN |
| Strength Number | .585 |
| Strength Unit | g/117g |
| Pharmaceutical Classes | Antiparasitic [EPC],Pediculicide [EPC] |
