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Terapie Anti-Fungal - 10849-002-01 - (MICONAZOLE NITRATE)

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Drug Information of Terapie Anti-Fungal

Product NDC: 10849-002
Proprietary Name: Terapie Anti-Fungal
Non Proprietary Name: MICONAZOLE NITRATE
Active Ingredient(s): 2    g/100g & nbsp;   MICONAZOLE NITRATE
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Terapie Anti-Fungal

Product NDC: 10849-002
Labeler Name: Armand Dupree Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333C
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20111104

Package Information of Terapie Anti-Fungal

Package NDC: 10849-002-01
Package Description: 1 TUBE in 1 CARTON (10849-002-01) > 60 g in 1 TUBE

NDC Information of Terapie Anti-Fungal

NDC Code 10849-002-01
Proprietary Name Terapie Anti-Fungal
Package Description 1 TUBE in 1 CARTON (10849-002-01) > 60 g in 1 TUBE
Product NDC 10849-002
Product Type Name HUMAN OTC DRUG
Non Proprietary Name MICONAZOLE NITRATE
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20111104
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Armand Dupree Inc.
Substance Name MICONAZOLE NITRATE
Strength Number 2
Strength Unit g/100g
Pharmaceutical Classes

Complete Information of Terapie Anti-Fungal


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