Product NDC: | 55289-824 |
Proprietary Name: | Fluconazole |
Non Proprietary Name: | Fluconazole |
Active Ingredient(s): | 200 mg/1 & nbsp; Fluconazole |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55289-824 |
Labeler Name: | PD-Rx Pharmaceuticals, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077253 |
Marketing Category: | ANDA |
Start Marketing Date: | 20060125 |
Package NDC: | 55289-824-20 |
Package Description: | 20 TABLET in 1 BOTTLE, PLASTIC (55289-824-20) |
NDC Code | 55289-824-20 |
Proprietary Name | Fluconazole |
Package Description | 20 TABLET in 1 BOTTLE, PLASTIC (55289-824-20) |
Product NDC | 55289-824 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Fluconazole |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20060125 |
Marketing Category Name | ANDA |
Labeler Name | PD-Rx Pharmaceuticals, Inc. |
Substance Name | FLUCONAZOLE |
Strength Number | 200 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |