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Fluconazole
Fluconazole - 49349-729-02 - (Fluconazole)
Drug Information of Fluconazole
| Product NDC: | 49349-729 |
| 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) |
Labeler Information of Fluconazole
| Product NDC: | 49349-729 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076042 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110823 |
Package Information of Fluconazole
| Package NDC: | 49349-729-02 |
| Package Description: | 30 TABLET in 1 BLISTER PACK (49349-729-02) |
NDC Information of Fluconazole
| NDC Code | 49349-729-02 |
| Proprietary Name | Fluconazole |
| Package Description | 30 TABLET in 1 BLISTER PACK (49349-729-02) |
| Product NDC | 49349-729 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fluconazole |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110823 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | FLUCONAZOLE |
| Strength Number | 150 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |
