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Ciclopirox
Ciclopirox - 0781-7106-60 - (Ciclopirox)
Drug Information of Ciclopirox
| Product NDC: | 0781-7106 |
| Proprietary Name: | Ciclopirox |
| Non Proprietary Name: | Ciclopirox |
| Active Ingredient(s): | 80 mg/g & nbsp; Ciclopirox |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ciclopirox
| Product NDC: | 0781-7106 |
| Labeler Name: | Sandoz |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077687 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070918 |
Package Information of Ciclopirox
| Package NDC: | 0781-7106-60 |
| Package Description: | 5.9136 g in 1 BOTTLE, WITH APPLICATOR (0781-7106-60) |
NDC Information of Ciclopirox
| NDC Code | 0781-7106-60 |
| Proprietary Name | Ciclopirox |
| Package Description | 5.9136 g in 1 BOTTLE, WITH APPLICATOR (0781-7106-60) |
| Product NDC | 0781-7106 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ciclopirox |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20070918 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz |
| Substance Name | CICLOPIROX |
| Strength Number | 80 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Decreased DNA Replication [PE],Decreased Protein Synthesis [PE],Decreased RNA Replication [PE],Protein Synthesis Inhibitors [MoA] |
