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Ciclopirox
Ciclopirox - 42192-705-01 - (Ciclopirox)
Drug Information of Ciclopirox
| Product NDC: | 42192-705 |
| Proprietary Name: | Ciclopirox |
| Non Proprietary Name: | Ciclopirox |
| Active Ingredient(s): | & nbsp; Ciclopirox |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ciclopirox
| Product NDC: | 42192-705 |
| Labeler Name: | Acella Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20090701 |
Package Information of Ciclopirox
| Package NDC: | 42192-705-01 |
| Package Description: | 1 KIT in 1 CARTON (42192-705-01) * 25 CLOTH in 1 PACKET * 1 GEL in 1 CAPSULE * 6.6 mL in 1 BOTTLE, GLASS |
NDC Information of Ciclopirox
| NDC Code | 42192-705-01 |
| Proprietary Name | Ciclopirox |
| Package Description | 1 KIT in 1 CARTON (42192-705-01) * 25 CLOTH in 1 PACKET * 1 GEL in 1 CAPSULE * 6.6 mL in 1 BOTTLE, GLASS |
| Product NDC | 42192-705 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Ciclopirox |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20090701 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Acella Pharmaceuticals, LLC |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
