Olanzapine - 66993-055-30 - (Olanzapine)

Alphabetical Index


Drug Information of Olanzapine

Product NDC: 66993-055
Proprietary Name: Olanzapine
Non Proprietary Name: Olanzapine
Active Ingredient(s): 15    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: 66993-055
Labeler Name: Prasco Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021086
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20111023

Package Information of Olanzapine

Package NDC: 66993-055-30
Package Description: 30 DOSE PACK in 1 CARTON (66993-055-30) > 1 BLISTER PACK in 1 DOSE PACK (66993-055-81) > 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

NDC Information of Olanzapine

NDC Code 66993-055-30
Proprietary Name Olanzapine
Package Description 30 DOSE PACK in 1 CARTON (66993-055-30) > 1 BLISTER PACK in 1 DOSE PACK (66993-055-81) > 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Product NDC 66993-055
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Olanzapine
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20111023
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Prasco Laboratories
Substance Name OLANZAPINE
Strength Number 15
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Olanzapine


General Information