Product NDC: | 54868-6116 |
Proprietary Name: | Fluconazole |
Non Proprietary Name: | fluconazole |
Active Ingredient(s): | 40 mg/mL & nbsp; fluconazole |
Administration Route(s): | ORAL |
Dosage Form(s): | POWDER, FOR SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-6116 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020090 |
Marketing Category: | NDA AUTHORIZED GENERIC |
Start Marketing Date: | 20100427 |
Package NDC: | 54868-6116-0 |
Package Description: | 1 BOTTLE in 1 CARTON (54868-6116-0) > 35 mL in 1 BOTTLE |
NDC Code | 54868-6116-0 |
Proprietary Name | Fluconazole |
Package Description | 1 BOTTLE in 1 CARTON (54868-6116-0) > 35 mL in 1 BOTTLE |
Product NDC | 54868-6116 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | fluconazole |
Dosage Form Name | POWDER, FOR SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 20100427 |
Marketing Category Name | NDA AUTHORIZED GENERIC |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | FLUCONAZOLE |
Strength Number | 40 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |