Product NDC: | 0066-8008 |
Proprietary Name: | Penlac |
Non Proprietary Name: | ciclopirox |
Active Ingredient(s): | 80 mg/mL & nbsp; ciclopirox |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0066-8008 |
Labeler Name: | Dermik Laboratories |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021022 |
Marketing Category: | NDA |
Start Marketing Date: | 19991217 |
Package NDC: | 0066-8008-01 |
Package Description: | 3.3 mL in 1 BOTTLE, WITH APPLICATOR (0066-8008-01) |
NDC Code | 0066-8008-01 |
Proprietary Name | Penlac |
Package Description | 3.3 mL in 1 BOTTLE, WITH APPLICATOR (0066-8008-01) |
Product NDC | 0066-8008 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | ciclopirox |
Dosage Form Name | SOLUTION |
Route Name | TOPICAL |
Start Marketing Date | 19991217 |
Marketing Category Name | NDA |
Labeler Name | Dermik Laboratories |
Substance Name | CICLOPIROX |
Strength Number | 80 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Decreased DNA Replication [PE],Decreased Protein Synthesis [PE],Decreased RNA Replication [PE],Protein Synthesis Inhibitors [MoA] |