Ciclopirox - 67405-450-66 - (Ciclopirox)

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Drug Information of Ciclopirox

Product NDC: 67405-450
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: 67405-450
Labeler Name: Harris Pharmaceutical, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078233
Marketing Category: ANDA
Start Marketing Date: 20070919

Package Information of Ciclopirox

Package NDC: 67405-450-66
Package Description: 6.6 mL in 1 BOTTLE, WITH APPLICATOR (67405-450-66)

NDC Information of Ciclopirox

NDC Code 67405-450-66
Proprietary Name Ciclopirox
Package Description 6.6 mL in 1 BOTTLE, WITH APPLICATOR (67405-450-66)
Product NDC 67405-450
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ciclopirox
Dosage Form Name SOLUTION
Route Name TOPICAL
Start Marketing Date 20070919
Marketing Category Name ANDA
Labeler Name Harris Pharmaceutical, 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