"43393-001-06" National Drug Code (NDC)

NDC Code	43393-001-06
Package Description	6 CARTON in 1 PACKAGE (43393-001-06) / 1 BLISTER PACK in 1 CARTON / 1 TABLET in 1 BLISTER PACK (43393-001-01)
Product NDC	43393-001
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Mifepristone
Non-Proprietary Name	Mifepristone
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20190501
Marketing Category Name	ANDA
Application Number	ANDA091178
Manufacturer	GenBioPro, Inc.
Substance Name	MIFEPRISTONE
Strength	200
Strength Unit	mg/1
Pharmacy Classes	Progestational Hormone Receptor Antagonists [MoA], Progestin Antagonist [EPC]