Product NDC: | 0472-0242 |
Proprietary Name: | Permethrin |
Non Proprietary Name: | Permethrin |
Active Ingredient(s): | 50 mg/g & nbsp; Permethrin |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0472-0242 |
Labeler Name: | Actavis Mid Atlantic LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA074806 |
Marketing Category: | ANDA |
Start Marketing Date: | 20041130 |
Package NDC: | 0472-0242-60 |
Package Description: | 1 TUBE in 1 CARTON (0472-0242-60) > 60 g in 1 TUBE |
NDC Code | 0472-0242-60 |
Proprietary Name | Permethrin |
Package Description | 1 TUBE in 1 CARTON (0472-0242-60) > 60 g in 1 TUBE |
Product NDC | 0472-0242 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Permethrin |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20041130 |
Marketing Category Name | ANDA |
Labeler Name | Actavis Mid Atlantic LLC |
Substance Name | PERMETHRIN |
Strength Number | 50 |
Strength Unit | mg/g |
Pharmaceutical Classes | Pyrethrins [Chemical/Ingredient],Pyrethroid [EPC] |