| Product NDC: | 0187-5180 | 
| 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: | 0187-5180 | 
| Labeler Name: | Valeant Pharmaceuticals North America LLC | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | NDA021022 | 
| Marketing Category: | NDA | 
| Start Marketing Date: | 20130501 | 
| Package NDC: | 0187-5180-06 | 
| Package Description: | 6.6 mL in 1 BOTTLE, WITH APPLICATOR (0187-5180-06) | 
| NDC Code | 0187-5180-06 | 
| Proprietary Name | Penlac | 
| Package Description | 6.6 mL in 1 BOTTLE, WITH APPLICATOR (0187-5180-06) | 
| Product NDC | 0187-5180 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | ciclopirox | 
| Dosage Form Name | SOLUTION | 
| Route Name | TOPICAL | 
| Start Marketing Date | 20130501 | 
| Marketing Category Name | NDA | 
| Labeler Name | Valeant Pharmaceuticals North America LLC | 
| 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] |