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FLUCONAZOLE
FLUCONAZOLE - 16590-283-30 - (FLUCONAZOLE)
Drug Information of FLUCONAZOLE
| Product NDC: | 16590-283 |
| Proprietary Name: | FLUCONAZOLE |
| Non Proprietary Name: | FLUCONAZOLE |
| Active Ingredient(s): | 200 mg/1 & nbsp; FLUCONAZOLE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of FLUCONAZOLE
| Product NDC: | 16590-283 |
| Labeler Name: | STAT Rx USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076077 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20040729 |
Package Information of FLUCONAZOLE
| Package NDC: | 16590-283-30 |
| Package Description: | 30 TABLET in 1 BOTTLE (16590-283-30) |
NDC Information of FLUCONAZOLE
| NDC Code | 16590-283-30 |
| Proprietary Name | FLUCONAZOLE |
| Package Description | 30 TABLET in 1 BOTTLE (16590-283-30) |
| Product NDC | 16590-283 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | FLUCONAZOLE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20040729 |
| Marketing Category Name | ANDA |
| Labeler Name | STAT Rx USA LLC |
| Substance Name | FLUCONAZOLE |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |
