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elimite
elimite - 40076-115-60 - (Permethrin)
Drug Information of elimite
| Product NDC: | 40076-115 |
| Proprietary Name: | elimite |
| Non Proprietary Name: | Permethrin |
| Active Ingredient(s): | 50 mg/100g & nbsp; Permethrin |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of elimite
| Product NDC: | 40076-115 |
| Labeler Name: | Prestium Pharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076369 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20121024 |
Package Information of elimite
| Package NDC: | 40076-115-60 |
| Package Description: | 1 TUBE in 1 CARTON (40076-115-60) > 60 g in 1 TUBE |
NDC Information of elimite
| NDC Code | 40076-115-60 |
| Proprietary Name | elimite |
| Package Description | 1 TUBE in 1 CARTON (40076-115-60) > 60 g in 1 TUBE |
| Product NDC | 40076-115 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Permethrin |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20121024 |
| Marketing Category Name | ANDA |
| Labeler Name | Prestium Pharma, Inc. |
| Substance Name | PERMETHRIN |
| Strength Number | 50 |
| Strength Unit | mg/100g |
| Pharmaceutical Classes | Pyrethrins [Chemical/Ingredient],Pyrethroid [EPC] |
