Ciclopirox - 0168-0449-04 - (Ciclopirox)

Alphabetical Index


Drug Information of Ciclopirox

Product NDC: 0168-0449
Proprietary Name: Ciclopirox
Non Proprietary Name: Ciclopirox
Active Ingredient(s): 10    mg/.96mL & nbsp;   Ciclopirox
Administration Route(s): TOPICAL
Dosage Form(s): SHAMPOO
Coding System: National Drug Codes(NDC)

Labeler Information of Ciclopirox

Product NDC: 0168-0449
Labeler Name: E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090146
Marketing Category: ANDA
Start Marketing Date: 20100525

Package Information of Ciclopirox

Package NDC: 0168-0449-04
Package Description: 1 BOTTLE in 1 CARTON (0168-0449-04) > 120 mL in 1 BOTTLE

NDC Information of Ciclopirox

NDC Code 0168-0449-04
Proprietary Name Ciclopirox
Package Description 1 BOTTLE in 1 CARTON (0168-0449-04) > 120 mL in 1 BOTTLE
Product NDC 0168-0449
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ciclopirox
Dosage Form Name SHAMPOO
Route Name TOPICAL
Start Marketing Date 20100525
Marketing Category Name ANDA
Labeler Name E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc.
Substance Name CICLOPIROX
Strength Number 10
Strength Unit mg/.96mL
Pharmaceutical Classes Decreased DNA Replication [PE],Decreased Protein Synthesis [PE],Decreased RNA Replication [PE],Protein Synthesis Inhibitors [MoA]

Complete Information of Ciclopirox


General Information