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] |