Olanzapine - 13668-090-05 - (Olanzapine)

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Drug Information of Olanzapine

Product NDC: 13668-090
Proprietary Name: Olanzapine
Non Proprietary Name: Olanzapine
Active Ingredient(s): 20    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: 13668-090
Labeler Name: Torrent Pharmaceuticals Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091415
Marketing Category: ANDA
Start Marketing Date: 20111025

Package Information of Olanzapine

Package NDC: 13668-090-05
Package Description: 500 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (13668-090-05)

NDC Information of Olanzapine

NDC Code 13668-090-05
Proprietary Name Olanzapine
Package Description 500 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (13668-090-05)
Product NDC 13668-090
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Olanzapine
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20111025
Marketing Category Name ANDA
Labeler Name Torrent Pharmaceuticals Limited
Substance Name OLANZAPINE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Olanzapine


General Information