"59392-6192-7" National Drug Code (NDC)

NDC Code	59392-6192-7
Package Description	500 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (59392-6192-7)
Product NDC	59392-6192
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Olanzapine
Non-Proprietary Name	Olanzapine
Dosage Form	TABLET, ORALLY DISINTEGRATING
Usage	ORAL
Start Marketing Date	20131201
Marketing Category Name	ANDA
Application Number	ANDA206892
Manufacturer	PharmTak, Inc.
Substance Name	OLANZAPINE
Strength	10
Strength Unit	mg/1
Pharmacy Classes	Atypical Antipsychotic [EPC]