Product NDC: | 68712-027 |
Proprietary Name: | CNL8 |
Non Proprietary Name: | Ciclopirox |
Active Ingredient(s): | 2.28 g/mL & nbsp; Ciclopirox |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68712-027 |
Labeler Name: | Innocutis Holdings LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA078270 |
Marketing Category: | ANDA |
Start Marketing Date: | 20081031 |
Package NDC: | 68712-027-01 |
Package Description: | 3 BOTTLE, GLASS in 1 CARTON (68712-027-01) > 5 mL in 1 BOTTLE, GLASS (68712-027-03) |
NDC Code | 68712-027-01 |
Proprietary Name | CNL8 |
Package Description | 3 BOTTLE, GLASS in 1 CARTON (68712-027-01) > 5 mL in 1 BOTTLE, GLASS (68712-027-03) |
Product NDC | 68712-027 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Ciclopirox |
Dosage Form Name | SOLUTION |
Route Name | TOPICAL |
Start Marketing Date | 20081031 |
Marketing Category Name | ANDA |
Labeler Name | Innocutis Holdings LLC |
Substance Name | CICLOPIROX |
Strength Number | 2.28 |
Strength Unit | g/mL |
Pharmaceutical Classes | Decreased DNA Replication [PE],Decreased Protein Synthesis [PE],Decreased RNA Replication [PE],Protein Synthesis Inhibitors [MoA] |