| Product NDC: | 68258-3036 | 
| Proprietary Name: | Fluconazole | 
| Non Proprietary Name: | Fluconazole | 
| Active Ingredient(s): | 150 mg/1 & nbsp; Fluconazole | 
| Administration Route(s): | ORAL | 
| Dosage Form(s): | TABLET | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 68258-3036 | 
| Labeler Name: | Dispensing Solutions Inc. | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | ANDA077253 | 
| Marketing Category: | ANDA | 
| Start Marketing Date: | 20040923 | 
| Package NDC: | 68258-3036-2 | 
| Package Description: | 2 BLISTER PACK in 1 CARTON (68258-3036-2) > 1 TABLET in 1 BLISTER PACK | 
| NDC Code | 68258-3036-2 | 
| Proprietary Name | Fluconazole | 
| Package Description | 2 BLISTER PACK in 1 CARTON (68258-3036-2) > 1 TABLET in 1 BLISTER PACK | 
| Product NDC | 68258-3036 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | Fluconazole | 
| Dosage Form Name | TABLET | 
| Route Name | ORAL | 
| Start Marketing Date | 20040923 | 
| Marketing Category Name | ANDA | 
| Labeler Name | Dispensing Solutions Inc. | 
| Substance Name | FLUCONAZOLE | 
| Strength Number | 150 | 
| Strength Unit | mg/1 | 
| Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |