Olanzapine - 60505-3113-0 - (Olanzapine)

Alphabetical Index


Drug Information of Olanzapine

Product NDC: 60505-3113
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: 60505-3113
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090798
Marketing Category: ANDA
Start Marketing Date: 20120423

Package Information of Olanzapine

Package NDC: 60505-3113-0
Package Description: 10 BLISTER PACK in 1 CARTON (60505-3113-0) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Olanzapine

NDC Code 60505-3113-0
Proprietary Name Olanzapine
Package Description 10 BLISTER PACK in 1 CARTON (60505-3113-0) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 60505-3113
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 Apotex Corp.
Substance Name OLANZAPINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Olanzapine


General Information