Zyprexa - 55154-1813-0 - (Olanzapine)

Alphabetical Index


Drug Information of Zyprexa

Product NDC: 55154-1813
Proprietary Name: Zyprexa
Non Proprietary Name: Olanzapine
Active Ingredient(s): 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: 55154-1813
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020592
Marketing Category: NDA
Start Marketing Date: 19961001

Package Information of Zyprexa

Package NDC: 55154-1813-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-1813-0) > 1 TABLET in 1 BLISTER PACK

NDC Information of Zyprexa

NDC Code 55154-1813-0
Proprietary Name Zyprexa
Package Description 10 BLISTER PACK in 1 BAG (55154-1813-0) > 1 TABLET in 1 BLISTER PACK
Product NDC 55154-1813
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Olanzapine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19961001
Marketing Category Name NDA
Labeler Name Cardinal Health
Substance Name OLANZAPINE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Zyprexa


General Information