Olanzapine - 49349-931-24 - (OLANZAPINE)

Alphabetical Index


Drug Information of Olanzapine

Product NDC: 49349-931
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: 49349-931
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076000
Marketing Category: ANDA
Start Marketing Date: 20121213

Package Information of Olanzapine

Package NDC: 49349-931-24
Package Description: 200 TABLET, FILM COATED in 1 CANISTER (49349-931-24)

NDC Information of Olanzapine

NDC Code 49349-931-24
Proprietary Name Olanzapine
Package Description 200 TABLET, FILM COATED in 1 CANISTER (49349-931-24)
Product NDC 49349-931
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name OLANZAPINE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20121213
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name OLANZAPINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Olanzapine


General Information