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Symbyax
Symbyax - 0002-3230-07 - (Olanzapine and Fluoxetine hydrochloride)
Drug Information of Symbyax
| Product NDC: | 0002-3230 |
| Proprietary Name: | Symbyax |
| Non Proprietary Name: | Olanzapine and Fluoxetine hydrochloride |
| Active Ingredient(s): | 25; 3 mg/1; mg/1 & nbsp; Olanzapine and Fluoxetine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Symbyax
| Product NDC: | 0002-3230 |
| Labeler Name: | Eli Lilly and Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021520 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20070409 |
Package Information of Symbyax
| Package NDC: | 0002-3230-07 |
| Package Description: | 7 CAPSULE in 1 BOTTLE (0002-3230-07) |
NDC Information of Symbyax
| NDC Code | 0002-3230-07 |
| Proprietary Name | Symbyax |
| Package Description | 7 CAPSULE in 1 BOTTLE (0002-3230-07) |
| Product NDC | 0002-3230 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Olanzapine and Fluoxetine hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20070409 |
| Marketing Category Name | NDA |
| Labeler Name | Eli Lilly and Company |
| Substance Name | FLUOXETINE HYDROCHLORIDE; OLANZAPINE |
| Strength Number | 25; 3 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Atypical Antipsychotic [EPC],Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
