Ciclopirox - 0168-0314-60 - (ciclopirox)

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Drug Information of Ciclopirox

Product NDC: 0168-0314
Proprietary Name: Ciclopirox
Non Proprietary Name: ciclopirox
Active Ingredient(s): 7.7    mg/mL & nbsp;   ciclopirox
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ciclopirox

Product NDC: 0168-0314
Labeler Name: E. FOUGERA & CO., A division of Fougera Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076422
Marketing Category: ANDA
Start Marketing Date: 20040806

Package Information of Ciclopirox

Package NDC: 0168-0314-60
Package Description: 60 mL in 1 BOTTLE (0168-0314-60)

NDC Information of Ciclopirox

NDC Code 0168-0314-60
Proprietary Name Ciclopirox
Package Description 60 mL in 1 BOTTLE (0168-0314-60)
Product NDC 0168-0314
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ciclopirox
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20040806
Marketing Category Name ANDA
Labeler Name E. FOUGERA & CO., A division of Fougera Pharmaceuticals Inc.
Substance Name CICLOPIROX OLAMINE
Strength Number 7.7
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