Olanzapine - 0904-6287-06 - (Olanzapine)

Alphabetical Index


Drug Information of Olanzapine

Product NDC: 0904-6287
Proprietary Name: Olanzapine
Non Proprietary Name: Olanzapine
Active Ingredient(s): 20    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: 0904-6287
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076133
Marketing Category: ANDA
Start Marketing Date: 20120423

Package Information of Olanzapine

Package NDC: 0904-6287-06
Package Description: 50 TABLET, FILM COATED in 1 BOX, UNIT-DOSE (0904-6287-06)

NDC Information of Olanzapine

NDC Code 0904-6287-06
Proprietary Name Olanzapine
Package Description 50 TABLET, FILM COATED in 1 BOX, UNIT-DOSE (0904-6287-06)
Product NDC 0904-6287
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Olanzapine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120423
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
Substance Name OLANZAPINE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Olanzapine


General Information