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Olanzapine and Fluoxetine - 49884-251-01 - (olanzapine and fuoxetine)

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Drug Information of Olanzapine and Fluoxetine

Product NDC: 49884-251
Proprietary Name: Olanzapine and Fluoxetine
Non Proprietary Name: olanzapine and fuoxetine
Active Ingredient(s): 50; 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: 49884-251
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: 49884-251-01
Package Description: 100 CAPSULE in 1 BOTTLE, PLASTIC (49884-251-01)

NDC Information of Olanzapine and Fluoxetine

NDC Code 49884-251-01
Proprietary Name Olanzapine and Fluoxetine
Package Description 100 CAPSULE in 1 BOTTLE, PLASTIC (49884-251-01)
Product NDC 49884-251
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 50; 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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