Home > National Drug Code (NDC) > Ciclopirox Olamine

Ciclopirox Olamine - 54868-5270-2 - (ciclopirox olamine)

Alphabetical Index


Drug Information of Ciclopirox Olamine

Product NDC: 54868-5270
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: 54868-5270
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076790
Marketing Category: ANDA
Start Marketing Date: 20050401

Package Information of Ciclopirox Olamine

Package NDC: 54868-5270-2
Package Description: 1 TUBE in 1 CARTON (54868-5270-2) > 30 g in 1 TUBE

NDC Information of Ciclopirox Olamine

NDC Code 54868-5270-2
Proprietary Name Ciclopirox Olamine
Package Description 1 TUBE in 1 CARTON (54868-5270-2) > 30 g in 1 TUBE
Product NDC 54868-5270
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ciclopirox olamine
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20050401
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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


General Information