Olanzapine - 0093-5105-05 - (Olanzapine)

Alphabetical Index


Drug Information of Olanzapine

Product NDC: 0093-5105
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: 0093-5105
Labeler Name: Teva Pharmaceuticals USA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076133
Marketing Category: ANDA
Start Marketing Date: 20111024

Package Information of Olanzapine

Package NDC: 0093-5105-05
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE (0093-5105-05)

NDC Information of Olanzapine

NDC Code 0093-5105-05
Proprietary Name Olanzapine
Package Description 500 TABLET, FILM COATED in 1 BOTTLE (0093-5105-05)
Product NDC 0093-5105
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Olanzapine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20111024
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA
Substance Name OLANZAPINE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Olanzapine


General Information