Ciclopirox - 61360-1351-8 - (ciclopirox)

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Drug Information of Ciclopirox

Product NDC: 61360-1351
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: 61360-1351
Labeler Name: Taro Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090269
Marketing Category: ANDA
Start Marketing Date: 20110223

Package Information of Ciclopirox

Package NDC: 61360-1351-8
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (61360-1351-8) > 120 mL in 1 BOTTLE, PLASTIC

NDC Information of Ciclopirox

NDC Code 61360-1351-8
Proprietary Name Ciclopirox
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (61360-1351-8) > 120 mL in 1 BOTTLE, PLASTIC
Product NDC 61360-1351
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ciclopirox
Dosage Form Name SHAMPOO
Route Name TOPICAL
Start Marketing Date 20110223
Marketing Category Name ANDA
Labeler Name Taro 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


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