| Product NDC: | 0703-1020 |
| Proprietary Name: | Fluconazole |
| Non Proprietary Name: | Fluconazole |
| Active Ingredient(s): | 400 mg/200mL & nbsp; Fluconazole |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0703-1020 |
| Labeler Name: | Teva Parenteral Medicines, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076837 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050316 |
| Package NDC: | 0703-1020-30 |
| Package Description: | 6 BAG in 1 CARTON (0703-1020-30) > 200 mL in 1 BAG (0703-1020-31) |
| NDC Code | 0703-1020-30 |
| Proprietary Name | Fluconazole |
| Package Description | 6 BAG in 1 CARTON (0703-1020-30) > 200 mL in 1 BAG (0703-1020-31) |
| Product NDC | 0703-1020 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fluconazole |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20050316 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Parenteral Medicines, Inc. |
| Substance Name | FLUCONAZOLE |
| Strength Number | 400 |
| Strength Unit | mg/200mL |
| Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |