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Sunmark Miconazole 7 - 49348-530-77 - (Miconazole nitrate)

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Drug Information of Sunmark Miconazole 7

Product NDC: 49348-530
Proprietary Name: Sunmark Miconazole 7
Non Proprietary Name: Miconazole nitrate
Active Ingredient(s): 2    g/100g & nbsp;   Miconazole nitrate
Administration Route(s): VAGINAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Sunmark Miconazole 7

Product NDC: 49348-530
Labeler Name: McKesson
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA074760
Marketing Category: ANDA
Start Marketing Date: 20030731

Package Information of Sunmark Miconazole 7

Package NDC: 49348-530-77
Package Description: 1 TUBE, WITH APPLICATOR in 1 CARTON (49348-530-77) > 45 g in 1 TUBE, WITH APPLICATOR

NDC Information of Sunmark Miconazole 7

NDC Code 49348-530-77
Proprietary Name Sunmark Miconazole 7
Package Description 1 TUBE, WITH APPLICATOR in 1 CARTON (49348-530-77) > 45 g in 1 TUBE, WITH APPLICATOR
Product NDC 49348-530
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Miconazole nitrate
Dosage Form Name CREAM
Route Name VAGINAL
Start Marketing Date 20030731
Marketing Category Name ANDA
Labeler Name McKesson
Substance Name MICONAZOLE NITRATE
Strength Number 2
Strength Unit g/100g
Pharmaceutical Classes

Complete Information of Sunmark Miconazole 7


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