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Diflucan
Diflucan - 0049-3450-19 - (FLUCONAZOLE)
Drug Information of Diflucan
| Product NDC: | 0049-3450 |
| Proprietary Name: | Diflucan |
| Non Proprietary Name: | FLUCONAZOLE |
| Active Ingredient(s): | 1400 mg/35mL & nbsp; FLUCONAZOLE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | POWDER, FOR SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Diflucan
| Product NDC: | 0049-3450 |
| Labeler Name: | Roerig |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020090 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19931223 |
Package Information of Diflucan
| Package NDC: | 0049-3450-19 |
| Package Description: | 35 mL in 1 BOTTLE (0049-3450-19) |
NDC Information of Diflucan
| NDC Code | 0049-3450-19 |
| Proprietary Name | Diflucan |
| Package Description | 35 mL in 1 BOTTLE (0049-3450-19) |
| Product NDC | 0049-3450 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | FLUCONAZOLE |
| Dosage Form Name | POWDER, FOR SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 19931223 |
| Marketing Category Name | NDA |
| Labeler Name | Roerig |
| Substance Name | FLUCONAZOLE |
| Strength Number | 1400 |
| Strength Unit | mg/35mL |
| Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |
