Product NDC: | 54868-5270 |
Proprietary Name: | Ciclopirox Olamine |
Non Proprietary Name: | ciclopirox olamine |
Active Ingredient(s): | 7.7 mg/g & nbsp; ciclopirox olamine |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-5270 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA076790 |
Marketing Category: | ANDA |
Start Marketing Date: | 20050401 |
Package NDC: | 54868-5270-1 |
Package Description: | 1 TUBE in 1 CARTON (54868-5270-1) > 15 g in 1 TUBE |
NDC Code | 54868-5270-1 |
Proprietary Name | Ciclopirox Olamine |
Package Description | 1 TUBE in 1 CARTON (54868-5270-1) > 15 g in 1 TUBE |
Product NDC | 54868-5270 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | ciclopirox olamine |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20050401 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | CICLOPIROX OLAMINE |
Strength Number | 7.7 |
Strength Unit | mg/g |
Pharmaceutical Classes | Decreased DNA Replication [PE],Decreased Protein Synthesis [PE],Decreased RNA Replication [PE],Protein Synthesis Inhibitors [MoA] |