Olanzapine - 0093-5771-01 - (Olanzapine)

Alphabetical Index


Drug Information of Olanzapine

Product NDC: 0093-5771
Proprietary Name: Olanzapine
Non Proprietary Name: Olanzapine
Active Ingredient(s): 15    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: 0093-5771
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076000
Marketing Category: ANDA
Start Marketing Date: 20111024

Package Information of Olanzapine

Package NDC: 0093-5771-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (0093-5771-01)

NDC Information of Olanzapine

NDC Code 0093-5771-01
Proprietary Name Olanzapine
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (0093-5771-01)
Product NDC 0093-5771
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 Inc
Substance Name OLANZAPINE
Strength Number 15
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Olanzapine


General Information