Olanzapine - 59746-307-32 - (Olanzapine)

Alphabetical Index


Drug Information of Olanzapine

Product NDC: 59746-307
Proprietary Name: Olanzapine
Non Proprietary Name: Olanzapine
Active Ingredient(s): 10    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: 59746-307
Labeler Name: Jubilant Cadista Pharmaceuticals Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200221
Marketing Category: ANDA
Start Marketing Date: 20120913

Package Information of Olanzapine

Package NDC: 59746-307-32
Package Description: 3 BLISTER PACK in 1 CARTON (59746-307-32) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (59746-307-12)

NDC Information of Olanzapine

NDC Code 59746-307-32
Proprietary Name Olanzapine
Package Description 3 BLISTER PACK in 1 CARTON (59746-307-32) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (59746-307-12)
Product NDC 59746-307
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Olanzapine
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20120913
Marketing Category Name ANDA
Labeler Name Jubilant Cadista Pharmaceuticals Inc
Substance Name OLANZAPINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Olanzapine


General Information