Home > National Drug Code (NDC) > Ciclopirox Olamine

Ciclopirox Olamine - 45802-400-49 - (Ciclopirox Olamine)

Alphabetical Index


Drug Information of Ciclopirox Olamine

Product NDC: 45802-400
Proprietary Name: Ciclopirox Olamine
Non Proprietary Name: Ciclopirox Olamine
Active Ingredient(s): 7.7    mg/100mL & nbsp;   Ciclopirox Olamine
Administration Route(s): TOPICAL
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Ciclopirox Olamine

Product NDC: 45802-400
Labeler Name: Perrigo New York Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077676
Marketing Category: ANDA
Start Marketing Date: 20061229

Package Information of Ciclopirox Olamine

Package NDC: 45802-400-49
Package Description: 1 BOTTLE in 1 CARTON (45802-400-49) > 30 mL in 1 BOTTLE

NDC Information of Ciclopirox Olamine

NDC Code 45802-400-49
Proprietary Name Ciclopirox Olamine
Package Description 1 BOTTLE in 1 CARTON (45802-400-49) > 30 mL in 1 BOTTLE
Product NDC 45802-400
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ciclopirox Olamine
Dosage Form Name SUSPENSION
Route Name TOPICAL
Start Marketing Date 20061229
Marketing Category Name ANDA
Labeler Name Perrigo New York Inc
Substance Name CICLOPIROX OLAMINE
Strength Number 7.7
Strength Unit mg/100mL
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