Desenex - 0067-0949-15 - (MICONAZOLE NITRATE)

Alphabetical Index


Drug Information of Desenex

Product NDC: 0067-0949
Proprietary Name: Desenex
Non Proprietary Name: MICONAZOLE NITRATE
Active Ingredient(s): 2    g/100g & nbsp;   MICONAZOLE NITRATE
Administration Route(s): TOPICAL
Dosage Form(s): POWDER
Coding System: National Drug Codes(NDC)

Labeler Information of Desenex

Product NDC: 0067-0949
Labeler Name: Novartis Consumer Health, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333C
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20090803

Package Information of Desenex

Package NDC: 0067-0949-15
Package Description: 43 g in 1 CONTAINER (0067-0949-15)

NDC Information of Desenex

NDC Code 0067-0949-15
Proprietary Name Desenex
Package Description 43 g in 1 CONTAINER (0067-0949-15)
Product NDC 0067-0949
Product Type Name HUMAN OTC DRUG
Non Proprietary Name MICONAZOLE NITRATE
Dosage Form Name POWDER
Route Name TOPICAL
Start Marketing Date 20090803
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Novartis Consumer Health, Inc.
Substance Name MICONAZOLE NITRATE
Strength Number 2
Strength Unit g/100g
Pharmaceutical Classes

Complete Information of Desenex


General Information