| Product NDC: | 68258-3996 | 
| 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: | 68258-3996 | 
| Labeler Name: | Dispensing Solutions, Inc. | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | ANDA090273 | 
| Marketing Category: | ANDA | 
| Start Marketing Date: | 20091113 | 
| Package NDC: | 68258-3996-3 | 
| Package Description: | 30 g in 1 CARTON (68258-3996-3) | 
| NDC Code | 68258-3996-3 | 
| Proprietary Name | Ciclopirox Olamine | 
| Package Description | 30 g in 1 CARTON (68258-3996-3) | 
| Product NDC | 68258-3996 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | Ciclopirox Olamine | 
| Dosage Form Name | CREAM | 
| Route Name | TOPICAL | 
| Start Marketing Date | 20091113 | 
| Marketing Category Name | ANDA | 
| Labeler Name | Dispensing Solutions, 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] |