| Product NDC: | 54868-5248 |
| Proprietary Name: | Fluconazole |
| Non Proprietary Name: | fluconazole |
| Active Ingredient(s): | 10 mg/mL & nbsp; fluconazole |
| Administration Route(s): | ORAL |
| Dosage Form(s): | POWDER, FOR SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 54868-5248 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020090 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20050311 |
| Package NDC: | 54868-5248-0 |
| Package Description: | 1 BOTTLE in 1 CARTON (54868-5248-0) > 35 mL in 1 BOTTLE |
| NDC Code | 54868-5248-0 |
| Proprietary Name | Fluconazole |
| Package Description | 1 BOTTLE in 1 CARTON (54868-5248-0) > 35 mL in 1 BOTTLE |
| Product NDC | 54868-5248 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | fluconazole |
| Dosage Form Name | POWDER, FOR SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20050311 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | FLUCONAZOLE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |