Olanzapine - 62756-757-66 - (Olanzapine)

Alphabetical Index


Drug Information of Olanzapine

Product NDC: 62756-757
Proprietary Name: Olanzapine
Non Proprietary Name: Olanzapine
Active Ingredient(s): 20    mg/1 & nbsp;   Olanzapine
Administration Route(s): ORAL
Dosage Form(s): TABLET, ORALLY DISINTEGRATING
Coding System: National Drug Codes(NDC)

Labeler Information of Olanzapine

Product NDC: 62756-757
Labeler Name: Sun Pharmaceutical Industries Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090881
Marketing Category: ANDA
Start Marketing Date: 20120228

Package Information of Olanzapine

Package NDC: 62756-757-66
Package Description: 1 BLISTER PACK in 1 CARTON (62756-757-66) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

NDC Information of Olanzapine

NDC Code 62756-757-66
Proprietary Name Olanzapine
Package Description 1 BLISTER PACK in 1 CARTON (62756-757-66) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Product NDC 62756-757
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Olanzapine
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20120228
Marketing Category Name ANDA
Labeler Name Sun Pharmaceutical Industries Limited
Substance Name OLANZAPINE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Olanzapine


General Information