"67253-902-50" National Drug Code (NDC)

NDC Code	67253-902-50
Package Description	500 TABLET in 1 BOTTLE (67253-902-50)
Product NDC	67253-902
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Alprazolam
Non-Proprietary Name	Alprazolam
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20070328
End Marketing Date	20220630
Marketing Category Name	ANDA
Application Number	ANDA074174
Manufacturer	Par Pharmaceutical
Substance Name	ALPRAZOLAM
Strength	1
Strength Unit	mg/1
Pharmacy Classes	Benzodiazepine [EPC], Benzodiazepines [CS]
DEA Schedule	CIV