Olanzapine - 52125-222-02 - (Olanzapine)

Alphabetical Index


Drug Information of Olanzapine

Product NDC: 52125-222
Proprietary Name: Olanzapine
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 Olanzapine

Product NDC: 52125-222
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091038
Marketing Category: ANDA
Start Marketing Date: 20130401

Package Information of Olanzapine

Package NDC: 52125-222-02
Package Description: 30 TABLET in 1 BLISTER PACK (52125-222-02)

NDC Information of Olanzapine

NDC Code 52125-222-02
Proprietary Name Olanzapine
Package Description 30 TABLET in 1 BLISTER PACK (52125-222-02)
Product NDC 52125-222
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Olanzapine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130401
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name OLANZAPINE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Olanzapine


General Information