Product NDC: | 0574-2059 |
Proprietary Name: | Ciclopirox |
Non Proprietary Name: | Ciclopirox |
Active Ingredient(s): | 10 mg/.96mL & nbsp; Ciclopirox |
Administration Route(s): | ORAL |
Dosage Form(s): | SHAMPOO |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0574-2059 |
Labeler Name: | Paddock Laboratories, LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA090490 |
Marketing Category: | ANDA |
Start Marketing Date: | 20091124 |
Package NDC: | 0574-2059-12 |
Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (0574-2059-12) > 120 mL in 1 BOTTLE, PLASTIC |
NDC Code | 0574-2059-12 |
Proprietary Name | Ciclopirox |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (0574-2059-12) > 120 mL in 1 BOTTLE, PLASTIC |
Product NDC | 0574-2059 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Ciclopirox |
Dosage Form Name | SHAMPOO |
Route Name | ORAL |
Start Marketing Date | 20091124 |
Marketing Category Name | ANDA |
Labeler Name | Paddock Laboratories, LLC |
Substance Name | CICLOPIROX |
Strength Number | 10 |
Strength Unit | mg/.96mL |
Pharmaceutical Classes | Decreased DNA Replication [PE],Decreased Protein Synthesis [PE],Decreased RNA Replication [PE],Protein Synthesis Inhibitors [MoA] |