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Fluconazole
Fluconazole - 0703-1019-03 - (Fluconazole)
Drug Information of Fluconazole
| Product NDC: | 0703-1019 |
| Proprietary Name: | Fluconazole |
| Non Proprietary Name: | Fluconazole |
| Active Ingredient(s): | 2 mg/mL & nbsp; Fluconazole |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fluconazole
| Product NDC: | 0703-1019 |
| Labeler Name: | Teva Parenteral Medicines, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076653 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20040805 |
Package Information of Fluconazole
| Package NDC: | 0703-1019-03 |
| Package Description: | 10 VIAL, SINGLE-DOSE in 1 CARTON (0703-1019-03) > 100 mL in 1 VIAL, SINGLE-DOSE (0703-1019-01) |
NDC Information of Fluconazole
| NDC Code | 0703-1019-03 |
| Proprietary Name | Fluconazole |
| Package Description | 10 VIAL, SINGLE-DOSE in 1 CARTON (0703-1019-03) > 100 mL in 1 VIAL, SINGLE-DOSE (0703-1019-01) |
| Product NDC | 0703-1019 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fluconazole |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20040805 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Parenteral Medicines, Inc. |
| Substance Name | FLUCONAZOLE |
| Strength Number | 2 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |
