Olanzapine - 16714-223-01 - (Olanzapine)

Alphabetical Index


Drug Information of Olanzapine

Product NDC: 16714-223
Proprietary Name: Olanzapine
Non Proprietary Name: Olanzapine
Active Ingredient(s): 20    mg/1 & nbsp;   Olanzapine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Olanzapine

Product NDC: 16714-223
Labeler Name: Northstar Rx LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202287
Marketing Category: ANDA
Start Marketing Date: 20120601

Package Information of Olanzapine

Package NDC: 16714-223-01
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (16714-223-01)

NDC Information of Olanzapine

NDC Code 16714-223-01
Proprietary Name Olanzapine
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (16714-223-01)
Product NDC 16714-223
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Olanzapine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120601
Marketing Category Name ANDA
Labeler Name Northstar Rx LLC
Substance Name OLANZAPINE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Olanzapine


General Information