Olanzapine - 0093-5247-65 - (Olanzapine)

Alphabetical Index


Drug Information of Olanzapine

Product NDC: 0093-5247
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: 0093-5247
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077243
Marketing Category: ANDA
Start Marketing Date: 20120224

Package Information of Olanzapine

Package NDC: 0093-5247-65
Package Description: 5 BLISTER PACK in 1 CARTON (0093-5247-65) > 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (0093-5247-19)

NDC Information of Olanzapine

NDC Code 0093-5247-65
Proprietary Name Olanzapine
Package Description 5 BLISTER PACK in 1 CARTON (0093-5247-65) > 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (0093-5247-19)
Product NDC 0093-5247
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Olanzapine
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20120224
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name OLANZAPINE
Strength Number 15
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Olanzapine


General Information