Ciclopirox - 0713-0317-87 - (Ciclopirox)

Alphabetical Index


Drug Information of Ciclopirox

Product NDC: 0713-0317
Proprietary Name: Ciclopirox
Non Proprietary Name: Ciclopirox
Active Ingredient(s): 80    mg/mL & nbsp;   Ciclopirox
Administration Route(s): TOPICAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ciclopirox

Product NDC: 0713-0317
Labeler Name: GW Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078233
Marketing Category: ANDA
Start Marketing Date: 20070522

Package Information of Ciclopirox

Package NDC: 0713-0317-87
Package Description: 3.3 mL in 1 BOTTLE, WITH APPLICATOR (0713-0317-87)

NDC Information of Ciclopirox

NDC Code 0713-0317-87
Proprietary Name Ciclopirox
Package Description 3.3 mL in 1 BOTTLE, WITH APPLICATOR (0713-0317-87)
Product NDC 0713-0317
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ciclopirox
Dosage Form Name SOLUTION
Route Name TOPICAL
Start Marketing Date 20070522
Marketing Category Name ANDA
Labeler Name GW Laboratories, Inc.
Substance Name CICLOPIROX
Strength Number 80
Strength Unit mg/mL
Pharmaceutical Classes Decreased DNA Replication [PE],Decreased Protein Synthesis [PE],Decreased RNA Replication [PE],Protein Synthesis Inhibitors [MoA]

Complete Information of Ciclopirox


General Information