Olanzapine - 66993-049-05 - (Olanzapine)

Alphabetical Index


Drug Information of Olanzapine

Product NDC: 66993-049
Proprietary Name: Olanzapine
Non Proprietary Name: Olanzapine
Active Ingredient(s): 7.5    mg/1 & nbsp;   Olanzapine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Olanzapine

Product NDC: 66993-049
Labeler Name: Prasco Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020592
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20111023

Package Information of Olanzapine

Package NDC: 66993-049-05
Package Description: 1 BOTTLE in 1 CARTON (66993-049-05) > 1000 TABLET in 1 BOTTLE

NDC Information of Olanzapine

NDC Code 66993-049-05
Proprietary Name Olanzapine
Package Description 1 BOTTLE in 1 CARTON (66993-049-05) > 1000 TABLET in 1 BOTTLE
Product NDC 66993-049
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Olanzapine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111023
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Prasco Laboratories
Substance Name OLANZAPINE
Strength Number 7.5
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Olanzapine


General Information