| NDC Code: |
0781-2191 |
| Proprietary Name: |
Olanzapine and Fluoxetine |
| Suffix: |
|
| Non-Proprietary Name: |
Olanzapine and Fluoxetine |
| Dosage Form: |
CAPSULE |
| Method: |
ORAL |
| Original Marketing Date: |
30-11-2012 |
| Category Name: |
ANDA |
| Application Number: |
ANDA078901 |
| Labeler: |
SANDOZ INC |
| Substance Name: |
FLUOXETINE HYDROCHLORIDE; OLANZAPINE |
| Active Numerator Strength: |
25; 6 |
| Active Ingredient Unit: |
mg/1; mg/1 |
| Pharm Classes: |
Atypical Antipsychotic [EPC],Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA] |
| DEA Schedule: |
|
