Loprox - 99207-013-30 - (CICLOPIROX)

Alphabetical Index


Drug Information of Loprox

Product NDC: 99207-013
Proprietary Name: Loprox
Non Proprietary Name: CICLOPIROX
Active Ingredient(s): 7.7    mg/g & nbsp;   CICLOPIROX
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Loprox

Product NDC: 99207-013
Labeler Name: Medicis Pharmaceutical Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020519
Marketing Category: NDA
Start Marketing Date: 20050501

Package Information of Loprox

Package NDC: 99207-013-30
Package Description: 1 TUBE in 1 CARTON (99207-013-30) > 30 g in 1 TUBE

NDC Information of Loprox

NDC Code 99207-013-30
Proprietary Name Loprox
Package Description 1 TUBE in 1 CARTON (99207-013-30) > 30 g in 1 TUBE
Product NDC 99207-013
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CICLOPIROX
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20050501
Marketing Category Name NDA
Labeler Name Medicis Pharmaceutical Corp
Substance Name CICLOPIROX
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 Loprox


General Information