"42582-200-20" National Drug Code (NDC)

NDC Code	42582-200-20
Package Description	1000 TABLET in 1 BOTTLE (42582-200-20)
Product NDC	42582-200
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Isoxsuprine Hydrochloride
Non-Proprietary Name	Isoxsuprine Hydrochloride
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20110602
Marketing Category Name	UNAPPROVED DRUG OTHER
Manufacturer	Bi-Coastal Pharmaceutical Corporation
Substance Name	ISOXSUPRINE HYDROCHLORIDE
Strength	20
Strength Unit	mg/1