Olanzapine - 0378-5335-93 - (olanzapine)

Alphabetical Index


Drug Information of Olanzapine

Product NDC: 0378-5335
Proprietary Name: Olanzapine
Non Proprietary Name: olanzapine
Active Ingredient(s): 7.5    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: 0378-5335
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076866
Marketing Category: ANDA
Start Marketing Date: 20130426

Package Information of Olanzapine

Package NDC: 0378-5335-93
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-5335-93)

NDC Information of Olanzapine

NDC Code 0378-5335-93
Proprietary Name Olanzapine
Package Description 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-5335-93)
Product NDC 0378-5335
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name olanzapine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130426
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
Substance Name OLANZAPINE
Strength Number 7.5
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Olanzapine


General Information