Product NDC: | 61748-200 |
Proprietary Name: | CICLOPIROX |
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: | 61748-200 |
Labeler Name: | VersaPharm Incorporated |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA078975 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100320 |
Package NDC: | 61748-200-06 |
Package Description: | 6.6 mL in 1 BOTTLE, WITH APPLICATOR (61748-200-06) |
NDC Code | 61748-200-06 |
Proprietary Name | CICLOPIROX |
Package Description | 6.6 mL in 1 BOTTLE, WITH APPLICATOR (61748-200-06) |
Product NDC | 61748-200 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | CICLOPIROX |
Dosage Form Name | SOLUTION |
Route Name | TOPICAL |
Start Marketing Date | 20100320 |
Marketing Category Name | ANDA |
Labeler Name | VersaPharm Incorporated |
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] |