Product NDC: | 59762-5034 |
Proprietary Name: | Fluconazole |
Non Proprietary Name: | fluconazole |
Active Ingredient(s): | 2 mg/mL & nbsp; fluconazole |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59762-5034 |
Labeler Name: | Greenstone LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA019950 |
Marketing Category: | NDA AUTHORIZED GENERIC |
Start Marketing Date: | 19900129 |
Package NDC: | 59762-5034-2 |
Package Description: | 6 CONTAINER in 1 CARTON (59762-5034-2) > 100 mL in 1 CONTAINER |
NDC Code | 59762-5034-2 |
Proprietary Name | Fluconazole |
Package Description | 6 CONTAINER in 1 CARTON (59762-5034-2) > 100 mL in 1 CONTAINER |
Product NDC | 59762-5034 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | fluconazole |
Dosage Form Name | SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 19900129 |
Marketing Category Name | NDA AUTHORIZED GENERIC |
Labeler Name | Greenstone LLC |
Substance Name | FLUCONAZOLE |
Strength Number | 2 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |