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Ciclopirox Olamine - 45802-138-18 - (Ciclopirox Olamine)

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Drug Information of Ciclopirox Olamine

Product NDC: 45802-138
Proprietary Name: Ciclopirox Olamine
Non Proprietary Name: Ciclopirox Olamine
Active Ingredient(s): 7.7    mg/g & nbsp;   Ciclopirox Olamine
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Ciclopirox Olamine

Product NDC: 45802-138
Labeler Name: Perrigo New York Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077364
Marketing Category: ANDA
Start Marketing Date: 20060719

Package Information of Ciclopirox Olamine

Package NDC: 45802-138-18
Package Description: 1 TUBE in 1 CARTON (45802-138-18) > 90 g in 1 TUBE

NDC Information of Ciclopirox Olamine

NDC Code 45802-138-18
Proprietary Name Ciclopirox Olamine
Package Description 1 TUBE in 1 CARTON (45802-138-18) > 90 g in 1 TUBE
Product NDC 45802-138
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ciclopirox Olamine
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20060719
Marketing Category Name ANDA
Labeler Name Perrigo New York Inc
Substance Name CICLOPIROX OLAMINE
Strength Number 7.7
Strength Unit mg/g
Pharmaceutical Classes Decreased DNA Replication [PE],Decreased Protein Synthesis [PE],Decreased RNA Replication [PE],Protein Synthesis Inhibitors [MoA]

Complete Information of Ciclopirox Olamine


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