Olanzapine - 54868-6364-0 - (Olanzapine)

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Drug Information of Olanzapine

Product NDC: 54868-6364
Proprietary Name: Olanzapine
Non Proprietary Name: Olanzapine
Active Ingredient(s): 7.5    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: 54868-6364
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076000
Marketing Category: ANDA
Start Marketing Date: 20120822

Package Information of Olanzapine

Package NDC: 54868-6364-0
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (54868-6364-0)

NDC Information of Olanzapine

NDC Code 54868-6364-0
Proprietary Name Olanzapine
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (54868-6364-0)
Product NDC 54868-6364
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Olanzapine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120822
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name OLANZAPINE
Strength Number 7.5
Strength Unit mg/1
Pharmaceutical Classes Atypical Antipsychotic [EPC]

Complete Information of Olanzapine


General Information