Ciclopirox - 42192-714-01 - (Ciclopirox)

Alphabetical Index


Drug Information of Ciclopirox

Product NDC: 42192-714
Proprietary Name: Ciclopirox
Non Proprietary Name: Ciclopirox
Active Ingredient(s):    & nbsp;   Ciclopirox
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of Ciclopirox

Product NDC: 42192-714
Labeler Name: Acella Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20110912

Package Information of Ciclopirox

Package NDC: 42192-714-01
Package Description: 1 KIT in 1 CARTON (42192-714-01) * 6.6 mL in 1 BOTTLE, WITH APPLICATOR * 28 mL in 1 BOTTLE

NDC Information of Ciclopirox

NDC Code 42192-714-01
Proprietary Name Ciclopirox
Package Description 1 KIT in 1 CARTON (42192-714-01) * 6.6 mL in 1 BOTTLE, WITH APPLICATOR * 28 mL in 1 BOTTLE
Product NDC 42192-714
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ciclopirox
Dosage Form Name KIT
Route Name
Start Marketing Date 20110912
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Acella Pharmaceuticals, LLC
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Ciclopirox


General Information