Olanzapine - 55111-163-78 - (Olanzapine)

Alphabetical Index


Drug Information of Olanzapine

Product NDC: 55111-163
Proprietary Name: Olanzapine
Non Proprietary Name: Olanzapine
Active Ingredient(s): 2.5    mg/1 & nbsp;   Olanzapine
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Olanzapine

Product NDC: 55111-163
Labeler Name: Dr.Reddy's laboratories Ltd.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076255
Marketing Category: ANDA
Start Marketing Date: 20120423

Package Information of Olanzapine

Package NDC: 55111-163-78
Package Description: 10 BLISTER PACK in 1 CARTON (55111-163-78) > 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-163-79)

NDC Information of Olanzapine

NDC Code 55111-163-78
Proprietary Name Olanzapine
Package Description 10 BLISTER PACK in 1 CARTON (55111-163-78) > 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-163-79)
Product NDC 55111-163
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Olanzapine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120423
Marketing Category Name ANDA
Labeler Name Dr.Reddy's laboratories Ltd.
Substance Name OLANZAPINE
Strength Number 2.5
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Olanzapine


General Information