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Olanzapine and Fluoxetine - 0093-5504-56 - (Olanzapine and Fluoxetine)

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Drug Information of Olanzapine and Fluoxetine

Product NDC: 0093-5504
Proprietary Name: Olanzapine and Fluoxetine
Non Proprietary Name: Olanzapine and Fluoxetine
Active Ingredient(s): 25; 6    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: 0093-5504
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: 0093-5504-56
Package Description: 30 CAPSULE in 1 BOTTLE (0093-5504-56)

NDC Information of Olanzapine and Fluoxetine

NDC Code 0093-5504-56
Proprietary Name Olanzapine and Fluoxetine
Package Description 30 CAPSULE in 1 BOTTLE (0093-5504-56)
Product NDC 0093-5504
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 25; 6
Strength Unit mg/1; mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC],Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

Complete Information of Olanzapine and Fluoxetine


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