Olanzapine - 52125-184-02 - (OLANZAPINE)

Alphabetical Index


Drug Information of Olanzapine

Product NDC: 52125-184
Proprietary Name: Olanzapine
Non Proprietary Name: OLANZAPINE
Active Ingredient(s): 10    mg/1 & nbsp;   OLANZAPINE
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Olanzapine

Product NDC: 52125-184
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076000
Marketing Category: ANDA
Start Marketing Date: 20130104

Package Information of Olanzapine

Package NDC: 52125-184-02
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (52125-184-02)

NDC Information of Olanzapine

NDC Code 52125-184-02
Proprietary Name Olanzapine
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (52125-184-02)
Product NDC 52125-184
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name OLANZAPINE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130104
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name OLANZAPINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Olanzapine


General Information