"42292-015-20" National Drug Code (NDC)

NDC Code	42292-015-20
Package Description	100 BLISTER PACK in 1 BOX, UNIT-DOSE (42292-015-20) > 1 TABLET in 1 BLISTER PACK (42292-015-01)
Product NDC	42292-015
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Olanzapine
Non-Proprietary Name	Olanzapine
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20160427
Marketing Category Name	ANDA
Application Number	ANDA202050
Manufacturer	Mylan Institutional Inc.
Substance Name	OLANZAPINE
Strength	15
Strength Unit	mg/1
Pharmacy Classes	Atypical Antipsychotic [EPC]