| Product NDC: | 0049-3371 |
| Proprietary Name: | Diflucan |
| Non Proprietary Name: | FLUCONAZOLE |
| Active Ingredient(s): | 2 mg/mL & nbsp; FLUCONAZOLE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0049-3371 |
| Labeler Name: | Roerig |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019950 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19900129 |
| Package NDC: | 0049-3371-26 |
| Package Description: | 6 BOTTLE, GLASS in 1 CARTON (0049-3371-26) > 100 mL in 1 BOTTLE, GLASS |
| NDC Code | 0049-3371-26 |
| Proprietary Name | Diflucan |
| Package Description | 6 BOTTLE, GLASS in 1 CARTON (0049-3371-26) > 100 mL in 1 BOTTLE, GLASS |
| Product NDC | 0049-3371 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | FLUCONAZOLE |
| Dosage Form Name | SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19900129 |
| Marketing Category Name | NDA |
| Labeler Name | Roerig |
| Substance Name | FLUCONAZOLE |
| Strength Number | 2 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |