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ciclopirox olamine - 0168-0313-15 - (ciclopirox olamine)

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Drug Information of ciclopirox olamine

Product NDC: 0168-0313
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: 0168-0313
Labeler Name: E. FOUGERA & CO. A division of Fougera Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076435
Marketing Category: ANDA
Start Marketing Date: 20041229

Package Information of ciclopirox olamine

Package NDC: 0168-0313-15
Package Description: 1 TUBE in 1 CARTON (0168-0313-15) > 15 g in 1 TUBE

NDC Information of ciclopirox olamine

NDC Code 0168-0313-15
Proprietary Name ciclopirox olamine
Package Description 1 TUBE in 1 CARTON (0168-0313-15) > 15 g in 1 TUBE
Product NDC 0168-0313
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ciclopirox olamine
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20041229
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/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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