Olanzapine - 62756-551-18 - (Olanzapine)

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Drug Information of Olanzapine

Product NDC: 62756-551
Proprietary Name: Olanzapine
Non Proprietary Name: Olanzapine
Active Ingredient(s): 2.5    mg/1 & nbsp;   Olanzapine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Olanzapine

Product NDC: 62756-551
Labeler Name: Sun Pharmaceutical Industries Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091038
Marketing Category: ANDA
Start Marketing Date: 20120423

Package Information of Olanzapine

Package NDC: 62756-551-18
Package Description: 1000 TABLET in 1 BOTTLE (62756-551-18)

NDC Information of Olanzapine

NDC Code 62756-551-18
Proprietary Name Olanzapine
Package Description 1000 TABLET in 1 BOTTLE (62756-551-18)
Product NDC 62756-551
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Olanzapine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120423
Marketing Category Name ANDA
Labeler Name Sun Pharmaceutical Industries Limited
Substance Name OLANZAPINE
Strength Number 2.5
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Olanzapine


General Information