Olanzapine - 49884-321-55 - (olanzapine)

Alphabetical Index


Drug Information of Olanzapine

Product NDC: 49884-321
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: 49884-321
Labeler Name: Par Pharmaceutical, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078109
Marketing Category: ANDA
Start Marketing Date: 20111024

Package Information of Olanzapine

Package NDC: 49884-321-55
Package Description: 3 BLISTER PACK in 1 CARTON (49884-321-55) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (49884-321-52)

NDC Information of Olanzapine

NDC Code 49884-321-55
Proprietary Name Olanzapine
Package Description 3 BLISTER PACK in 1 CARTON (49884-321-55) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (49884-321-52)
Product NDC 49884-321
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name olanzapine
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20111024
Marketing Category Name ANDA
Labeler Name Par Pharmaceutical, Inc.
Substance Name OLANZAPINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Olanzapine


General Information