ZYPREXA - 0002-4456-07 - (Olanzapine)

Alphabetical Index


Drug Information of ZYPREXA

Product NDC: 0002-4456
Proprietary Name: ZYPREXA
Non Proprietary Name: Olanzapine
Active Ingredient(s): 20    mg/1 & nbsp;   Olanzapine
Administration Route(s): ORAL
Dosage Form(s): TABLET, ORALLY DISINTEGRATING
Coding System: National Drug Codes(NDC)

Labeler Information of ZYPREXA

Product NDC: 0002-4456
Labeler Name: Eli Lilly and Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021086
Marketing Category: NDA
Start Marketing Date: 20010901

Package Information of ZYPREXA

Package NDC: 0002-4456-07
Package Description: 7 DOSE PACK in 1 CARTON (0002-4456-07) > 1 BLISTER PACK in 1 DOSE PACK > 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

NDC Information of ZYPREXA

NDC Code 0002-4456-07
Proprietary Name ZYPREXA
Package Description 7 DOSE PACK in 1 CARTON (0002-4456-07) > 1 BLISTER PACK in 1 DOSE PACK > 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Product NDC 0002-4456
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Olanzapine
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20010901
Marketing Category Name NDA
Labeler Name Eli Lilly and Company
Substance Name OLANZAPINE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of ZYPREXA


General Information