Zyprexa - 24236-975-35 - (Olanzapine)

Alphabetical Index


Drug Information of Zyprexa

Product NDC: 24236-975
Proprietary Name: Zyprexa
Non Proprietary Name: Olanzapine
Active Ingredient(s): 15    mg/1 & nbsp;   Olanzapine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Zyprexa

Product NDC: 24236-975
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020592
Marketing Category: NDA
Start Marketing Date: 20130514

Package Information of Zyprexa

Package NDC: 24236-975-35
Package Description: 30 TABLET in 1 CANISTER (24236-975-35)

NDC Information of Zyprexa

NDC Code 24236-975-35
Proprietary Name Zyprexa
Package Description 30 TABLET in 1 CANISTER (24236-975-35)
Product NDC 24236-975
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Olanzapine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130514
Marketing Category Name NDA
Labeler Name REMEDYREPACK INC.
Substance Name OLANZAPINE
Strength Number 15
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Zyprexa


General Information