Ciclopirox - 0574-2059-12 - (Ciclopirox)

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Drug Information of Ciclopirox

Product NDC: 0574-2059
Proprietary Name: Ciclopirox
Non Proprietary Name: Ciclopirox
Active Ingredient(s): 10    mg/.96mL & nbsp;   Ciclopirox
Administration Route(s): ORAL
Dosage Form(s): SHAMPOO
Coding System: National Drug Codes(NDC)

Labeler Information of Ciclopirox

Product NDC: 0574-2059
Labeler Name: Paddock Laboratories, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090490
Marketing Category: ANDA
Start Marketing Date: 20091124

Package Information of Ciclopirox

Package NDC: 0574-2059-12
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (0574-2059-12) > 120 mL in 1 BOTTLE, PLASTIC

NDC Information of Ciclopirox

NDC Code 0574-2059-12
Proprietary Name Ciclopirox
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (0574-2059-12) > 120 mL in 1 BOTTLE, PLASTIC
Product NDC 0574-2059
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ciclopirox
Dosage Form Name SHAMPOO
Route Name ORAL
Start Marketing Date 20091124
Marketing Category Name ANDA
Labeler Name Paddock Laboratories, LLC
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