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Medicated Anti-Fungal Miconazole - 68754-150-00 - (Miconazole Nitrate)

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Drug Information of Medicated Anti-Fungal Miconazole

Product NDC: 68754-150
Proprietary Name: Medicated Anti-Fungal Miconazole
Non Proprietary Name: Miconazole Nitrate
Active Ingredient(s): 2    g/100g & nbsp;   Miconazole Nitrate
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Medicated Anti-Fungal Miconazole

Product NDC: 68754-150
Labeler Name: American Spraytech, LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: part333
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100602

Package Information of Medicated Anti-Fungal Miconazole

Package NDC: 68754-150-00
Package Description: 150 g in 1 CAN (68754-150-00)

NDC Information of Medicated Anti-Fungal Miconazole

NDC Code 68754-150-00
Proprietary Name Medicated Anti-Fungal Miconazole
Package Description 150 g in 1 CAN (68754-150-00)
Product NDC 68754-150
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Miconazole Nitrate
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20100602
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name American Spraytech, LLC
Substance Name MICONAZOLE NITRATE
Strength Number 2
Strength Unit g/100g
Pharmaceutical Classes

Complete Information of Medicated Anti-Fungal Miconazole


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