Zyprexa - 52959-579-30 - (Olanzapine)

Alphabetical Index


Drug Information of Zyprexa

Product NDC: 52959-579
Proprietary Name: Zyprexa
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 Zyprexa

Product NDC: 52959-579
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020592
Marketing Category: NDA
Start Marketing Date: 19970623

Package Information of Zyprexa

Package NDC: 52959-579-30
Package Description: 30 TABLET in 1 BOTTLE (52959-579-30)

NDC Information of Zyprexa

NDC Code 52959-579-30
Proprietary Name Zyprexa
Package Description 30 TABLET in 1 BOTTLE (52959-579-30)
Product NDC 52959-579
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Olanzapine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19970623
Marketing Category Name NDA
Labeler Name H.J. Harkins Company, Inc.
Substance Name OLANZAPINE
Strength Number 2.5
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Zyprexa


General Information