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Permethrin
Permethrin - 21695-907-60 - (Permethrin)
Drug Information of Permethrin
| Product NDC: | 21695-907 |
| 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) |
Labeler Information of Permethrin
| Product NDC: | 21695-907 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076369 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20030421 |
Package Information of Permethrin
| Package NDC: | 21695-907-60 |
| Package Description: | 60 g in 1 TUBE (21695-907-60) |
NDC Information of Permethrin
| NDC Code | 21695-907-60 |
| Proprietary Name | Permethrin |
| Package Description | 60 g in 1 TUBE (21695-907-60) |
| Product NDC | 21695-907 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Permethrin |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20030421 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | PERMETHRIN |
| Strength Number | 50 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Pyrethrins [Chemical/Ingredient],Pyrethroid [EPC] |
