Product NDC: | 54868-5345 |
Proprietary Name: | Fluconazole |
Non Proprietary Name: | fluconazole |
Active Ingredient(s): | 100 mg/1 & nbsp; fluconazole |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-5345 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA019949 |
Marketing Category: | NDA AUTHORIZED GENERIC |
Start Marketing Date: | 20050706 |
Package NDC: | 54868-5345-7 |
Package Description: | 3 TABLET in 1 BOTTLE, PLASTIC (54868-5345-7) |
NDC Code | 54868-5345-7 |
Proprietary Name | Fluconazole |
Package Description | 3 TABLET in 1 BOTTLE, PLASTIC (54868-5345-7) |
Product NDC | 54868-5345 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | fluconazole |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20050706 |
Marketing Category Name | NDA AUTHORIZED GENERIC |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | FLUCONAZOLE |
Strength Number | 100 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |