Zyprexa - 0002-4116-33 - (Olanzapine)

Alphabetical Index


Drug Information of Zyprexa

Product NDC: 0002-4116
Proprietary Name: Zyprexa
Non Proprietary Name: Olanzapine
Active Ingredient(s): 7.5    mg/1 & nbsp;   Olanzapine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Zyprexa

Product NDC: 0002-4116
Labeler Name: Eli Lilly and Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020592
Marketing Category: NDA
Start Marketing Date: 19961001

Package Information of Zyprexa

Package NDC: 0002-4116-33
Package Description: 100 BLISTER PACK in 1 CARTON (0002-4116-33) > 1 TABLET in 1 BLISTER PACK (0002-4116-01)

NDC Information of Zyprexa

NDC Code 0002-4116-33
Proprietary Name Zyprexa
Package Description 100 BLISTER PACK in 1 CARTON (0002-4116-33) > 1 TABLET in 1 BLISTER PACK (0002-4116-01)
Product NDC 0002-4116
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 Eli Lilly and Company
Substance Name OLANZAPINE
Strength Number 7.5
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Zyprexa


General Information