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Ulesfia
Ulesfia - 59630-780-08 - (benzyl alcohol)
Drug Information of Ulesfia
| Product NDC: | 59630-780 |
| Proprietary Name: | Ulesfia |
| Non Proprietary Name: | benzyl alcohol |
| Active Ingredient(s): | 50 mg/g & nbsp; benzyl alcohol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ulesfia
| Product NDC: | 59630-780 |
| Labeler Name: | Shionogi Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022129 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090526 |
Package Information of Ulesfia
| Package NDC: | 59630-780-08 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (59630-780-08) > 227 g in 1 BOTTLE, PLASTIC |
NDC Information of Ulesfia
| NDC Code | 59630-780-08 |
| Proprietary Name | Ulesfia |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (59630-780-08) > 227 g in 1 BOTTLE, PLASTIC |
| Product NDC | 59630-780 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | benzyl alcohol |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20090526 |
| Marketing Category Name | NDA |
| Labeler Name | Shionogi Inc. |
| Substance Name | BENZYL ALCOHOL |
| Strength Number | 50 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Pediculicide [EPC] |
