| 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] |