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Olanzapine and Fluoxetine
Olanzapine and Fluoxetine - 0093-5507-56 - (Olanzapine and Fluoxetine)
Drug Information of Olanzapine and Fluoxetine
| Product NDC: | 0093-5507 |
| Proprietary Name: | Olanzapine and Fluoxetine |
| Non Proprietary Name: | Olanzapine and Fluoxetine |
| Active Ingredient(s): | 50; 12 mg/1; mg/1 & nbsp; Olanzapine and Fluoxetine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Olanzapine and Fluoxetine
| Product NDC: | 0093-5507 |
| Labeler Name: | Teva Pharmaceuticals USA Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077528 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120619 |
Package Information of Olanzapine and Fluoxetine
| Package NDC: | 0093-5507-56 |
| Package Description: | 30 CAPSULE in 1 BOTTLE (0093-5507-56) |
NDC Information of Olanzapine and Fluoxetine
| NDC Code | 0093-5507-56 |
| Proprietary Name | Olanzapine and Fluoxetine |
| Package Description | 30 CAPSULE in 1 BOTTLE (0093-5507-56) |
| Product NDC | 0093-5507 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Olanzapine and Fluoxetine |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20120619 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Pharmaceuticals USA Inc |
| Substance Name | FLUOXETINE HYDROCHLORIDE; OLANZAPINE |
| Strength Number | 50; 12 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Atypical Antipsychotic [EPC],Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
