"48792-7855-1" National Drug Code (NDC)

NDC Code	48792-7855-1
Package Description	30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (48792-7855-1)
Product NDC	48792-7855
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Olanzapine
Non-Proprietary Name	Olanzapine
Dosage Form	TABLET, ORALLY DISINTEGRATING
Usage	ORAL
Start Marketing Date	20180710
Marketing Category Name	ANDA
Application Number	ANDA208146
Manufacturer	Sunshine Lake Pharma Co., Ltd.
Substance Name	OLANZAPINE
Strength	5
Strength Unit	mg/1
Pharmacy Classes	Atypical Antipsychotic [EPC]