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Diflucan
Diflucan - 52125-223-02 - (fluconazole)
Drug Information of Diflucan
| Product NDC: | 52125-223 |
| Proprietary Name: | Diflucan |
| Non Proprietary Name: | fluconazole |
| Active Ingredient(s): | 100 mg/1 & nbsp; fluconazole |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Diflucan
| Product NDC: | 52125-223 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019949 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20130219 |
Package Information of Diflucan
| Package NDC: | 52125-223-02 |
| Package Description: | 30 TABLET in 1 BLISTER PACK (52125-223-02) |
NDC Information of Diflucan
| NDC Code | 52125-223-02 |
| Proprietary Name | Diflucan |
| Package Description | 30 TABLET in 1 BLISTER PACK (52125-223-02) |
| Product NDC | 52125-223 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | fluconazole |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130219 |
| Marketing Category Name | NDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | FLUCONAZOLE |
| Strength Number | 100 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |
