| Product NDC: | 0143-9668 |
| Proprietary Name: | Fluconazole |
| Non Proprietary Name: | Fluconazole |
| Active Ingredient(s): | 2 mg/mL & nbsp; Fluconazole |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0143-9668 |
| Labeler Name: | West-ward Pharmaceutical Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078698 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120130 |
| Package NDC: | 0143-9668-06 |
| Package Description: | 6 CONTAINER in 1 CARTON (0143-9668-06) > 200 mL in 1 CONTAINER (0143-9668-01) |
| NDC Code | 0143-9668-06 |
| Proprietary Name | Fluconazole |
| Package Description | 6 CONTAINER in 1 CARTON (0143-9668-06) > 200 mL in 1 CONTAINER (0143-9668-01) |
| Product NDC | 0143-9668 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fluconazole |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20120130 |
| Marketing Category Name | ANDA |
| Labeler Name | West-ward Pharmaceutical Corp |
| Substance Name | FLUCONAZOLE |
| Strength Number | 2 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |