| Product NDC: | 66336-570 | 
| 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: | 66336-570 | 
| Labeler Name: | Dispensing Solutions, Inc. | 
| Product Type: | HUMAN PRESCRIPTION DRUG | 
| FDA Application Number: | ANDA076077 | 
| Marketing Category: | ANDA | 
| Start Marketing Date: | 20101201 | 
| Package NDC: | 66336-570-11 | 
| Package Description: | 11 TABLET in 1 BOTTLE (66336-570-11) | 
| NDC Code | 66336-570-11 | 
| Proprietary Name | Fluconazole | 
| Package Description | 11 TABLET in 1 BOTTLE (66336-570-11) | 
| Product NDC | 66336-570 | 
| Product Type Name | HUMAN PRESCRIPTION DRUG | 
| Non Proprietary Name | Fluconazole | 
| Dosage Form Name | TABLET | 
| Route Name | ORAL | 
| Start Marketing Date | 20101201 | 
| Marketing Category Name | ANDA | 
| Labeler Name | Dispensing Solutions, Inc. | 
| Substance Name | FLUCONAZOLE | 
| Strength Number | 100 | 
| Strength Unit | mg/1 | 
| Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |