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Dynarex Antifungal - 67777-231-02 - (antifungal)

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Drug Information of Dynarex Antifungal

Product NDC: 67777-231
Proprietary Name: Dynarex Antifungal
Non Proprietary Name: antifungal
Active Ingredient(s): 1    g/100g & nbsp;   antifungal
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Dynarex Antifungal

Product NDC: 67777-231
Labeler Name: Dynarex Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part333C
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100518

Package Information of Dynarex Antifungal

Package NDC: 67777-231-02
Package Description: 28.25 g in 1 TUBE (67777-231-02)

NDC Information of Dynarex Antifungal

NDC Code 67777-231-02
Proprietary Name Dynarex Antifungal
Package Description 28.25 g in 1 TUBE (67777-231-02)
Product NDC 67777-231
Product Type Name HUMAN OTC DRUG
Non Proprietary Name antifungal
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20100518
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Dynarex Corporation
Substance Name CLOTRIMAZOLE
Strength Number 1
Strength Unit g/100g
Pharmaceutical Classes

Complete Information of Dynarex Antifungal


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