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Fluconazole
Fluconazole - 59762-5015-1 - (fluconazole)
Drug Information of Fluconazole
| Product NDC: | 59762-5015 |
| Proprietary Name: | Fluconazole |
| Non Proprietary Name: | fluconazole |
| Active Ingredient(s): | 50 mg/1 & nbsp; fluconazole |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fluconazole
| Product NDC: | 59762-5015 |
| Labeler Name: | Greenstone LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019949 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 19900129 |
Package Information of Fluconazole
| Package NDC: | 59762-5015-1 |
| Package Description: | 30 TABLET in 1 BOTTLE (59762-5015-1) |
NDC Information of Fluconazole
| NDC Code | 59762-5015-1 |
| Proprietary Name | Fluconazole |
| Package Description | 30 TABLET in 1 BOTTLE (59762-5015-1) |
| Product NDC | 59762-5015 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | fluconazole |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19900129 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Greenstone LLC |
| Substance Name | FLUCONAZOLE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |
