"0781-5377-05" National Drug Code (NDC)

NDC Code	0781-5377-05
Package Description	500 TABLET in 1 BOTTLE (0781-5377-05)
Product NDC	0781-5377
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Lorazepam
Non-Proprietary Name	Lorazepam
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20070104
End Marketing Date	20210930
Marketing Category Name	ANDA
Application Number	ANDA071141
Manufacturer	Sandoz Inc
Substance Name	LORAZEPAM
Strength	1
Strength Unit	mg/1
Pharmacy Classes	Benzodiazepine [EPC],Benzodiazepines [CS]
DEA Schedule	CIV