"70518-0162-3" National Drug Code (NDC)

NDC Code	70518-0162-3
Package Description	2 TABLET in 1 BOTTLE, PLASTIC (70518-0162-3)
Product NDC	70518-0162
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Diazepam
Non-Proprietary Name	Diazepam
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20170123
Marketing Category Name	ANDA
Application Number	ANDA071322
Manufacturer	REMEDYREPACK INC.
Substance Name	DIAZEPAM
Strength	10
Strength Unit	mg/1
Pharmacy Classes	Benzodiazepine [EPC], Benzodiazepines [CS]
DEA Schedule	CIV