Product NDC: | 0143-9899 |
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: | 0143-9899 |
Labeler Name: | West-ward Pharmaceutical Corp |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA076736 |
Marketing Category: | ANDA |
Start Marketing Date: | 20050823 |
Package NDC: | 0143-9899-91 |
Package Description: | 6 VIAL in 1 CARTON (0143-9899-91) > 100 mL in 1 VIAL (0143-9899-01) |
NDC Code | 0143-9899-91 |
Proprietary Name | Fluconazole |
Package Description | 6 VIAL in 1 CARTON (0143-9899-91) > 100 mL in 1 VIAL (0143-9899-01) |
Product NDC | 0143-9899 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Fluconazole |
Dosage Form Name | INJECTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20050823 |
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] |