Olanzapine - 66993-466-30 - (Olanzapine)

Alphabetical Index


Drug Information of Olanzapine

Product NDC: 66993-466
Proprietary Name: Olanzapine
Non Proprietary Name: Olanzapine
Active Ingredient(s): 5    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: 66993-466
Labeler Name: Prasco Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091415
Marketing Category: ANDA
Start Marketing Date: 20120515

Package Information of Olanzapine

Package NDC: 66993-466-30
Package Description: 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (66993-466-30)

NDC Information of Olanzapine

NDC Code 66993-466-30
Proprietary Name Olanzapine
Package Description 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (66993-466-30)
Product NDC 66993-466
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Olanzapine
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20120515
Marketing Category Name ANDA
Labeler Name Prasco Laboratories
Substance Name OLANZAPINE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Olanzapine


General Information