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Olanzapine and Fluoxetine
Olanzapine and Fluoxetine - 49884-250-01 - (olanzapine and fuoxetine)
Drug Information of Olanzapine and Fluoxetine
| Product NDC: | 49884-250 |
| Proprietary Name: | Olanzapine and Fluoxetine |
| Non Proprietary Name: | olanzapine and fuoxetine |
| Active Ingredient(s): | 25; 6 mg/1; mg/1 & nbsp; olanzapine and fuoxetine |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Olanzapine and Fluoxetine
| Product NDC: | 49884-250 |
| Labeler Name: | Par Pharmaceutical, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077742 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20121128 |
Package Information of Olanzapine and Fluoxetine
| Package NDC: | 49884-250-01 |
| Package Description: | 100 CAPSULE in 1 BOTTLE, PLASTIC (49884-250-01) |
NDC Information of Olanzapine and Fluoxetine
| NDC Code | 49884-250-01 |
| Proprietary Name | Olanzapine and Fluoxetine |
| Package Description | 100 CAPSULE in 1 BOTTLE, PLASTIC (49884-250-01) |
| Product NDC | 49884-250 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | olanzapine and fuoxetine |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20121128 |
| Marketing Category Name | ANDA |
| Labeler Name | Par Pharmaceutical, Inc |
| Substance Name | FLUOXETINE HYDROCHLORIDE; OLANZAPINE |
| Strength Number | 25; 6 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Atypical Antipsychotic [EPC],Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
