Product NDC: | 61360-1351 |
Proprietary Name: | Ciclopirox |
Non Proprietary Name: | ciclopirox |
Active Ingredient(s): | 10 mg/.96mL & nbsp; ciclopirox |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SHAMPOO |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 61360-1351 |
Labeler Name: | Taro Pharmaceuticals, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA090269 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110223 |
Package NDC: | 61360-1351-8 |
Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (61360-1351-8) > 120 mL in 1 BOTTLE, PLASTIC |
NDC Code | 61360-1351-8 |
Proprietary Name | Ciclopirox |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (61360-1351-8) > 120 mL in 1 BOTTLE, PLASTIC |
Product NDC | 61360-1351 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | ciclopirox |
Dosage Form Name | SHAMPOO |
Route Name | TOPICAL |
Start Marketing Date | 20110223 |
Marketing Category Name | ANDA |
Labeler Name | Taro Pharmaceuticals, Inc. |
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] |