Product NDC: | 43538-501 |
Proprietary Name: | Ciclodan |
Non Proprietary Name: | ciclopirox |
Active Ingredient(s): | 2.28 g/mL & nbsp; ciclopirox |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 43538-501 |
Labeler Name: | Medimetriks Pharmaceuticals, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA078233 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110410 |
Package NDC: | 43538-501-06 |
Package Description: | 1 BOTTLE, WITH APPLICATOR in 1 KIT (43538-501-06) > 6.6 mL in 1 BOTTLE, WITH APPLICATOR |
NDC Code | 43538-501-06 |
Proprietary Name | Ciclodan |
Package Description | 1 BOTTLE, WITH APPLICATOR in 1 KIT (43538-501-06) > 6.6 mL in 1 BOTTLE, WITH APPLICATOR |
Product NDC | 43538-501 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | ciclopirox |
Dosage Form Name | SOLUTION |
Route Name | TOPICAL |
Start Marketing Date | 20110410 |
Marketing Category Name | ANDA |
Labeler Name | Medimetriks Pharmaceuticals, Inc. |
Substance Name | CICLOPIROX |
Strength Number | 2.28 |
Strength Unit | g/mL |
Pharmaceutical Classes | Decreased DNA Replication [PE],Decreased Protein Synthesis [PE],Decreased RNA Replication [PE],Protein Synthesis Inhibitors [MoA] |