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] |