"64720-321-50" National Drug Code (NDC)

NDC Code	64720-321-50
Package Description	500 TABLET in 1 BOTTLE (64720-321-50)
Product NDC	64720-321
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Metaxalone
Non-Proprietary Name	Metaxalone
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20071101
End Marketing Date	20200401
Marketing Category Name	NDA
Application Number	NDA013217
Manufacturer	CorePharma, LLC
Substance Name	METAXALONE
Strength	800
Strength Unit	mg/1
Pharmacy Classes	Centrally-mediated Muscle Relaxation [PE]