美国药品NDC（国家药品编码）与药品说明书数据库（U.S. FDA National Drug Code DataBase）

NDC包装代码	产品NDC	产品类型	商品名	通用名	剂型	给药途径	上市日期	结束日期	市场类别	申请号	标签持有者	活性成分	规格	包装描述
60687-620-01	60687-620	HUMAN PRESCRIPTION DRUG	Metoclopramide	Metoclopramide	TABLET	ORAL	20211111	N/A	ANDA	ANDA072801	American Health Packaging	METOCLOPRAMIDE HYDROCHLORIDE	5 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-620-01) / 1 TABLET in 1 BLISTER PACK (60687-620-11)
55154-4383-0	55154-4383	HUMAN PRESCRIPTION DRUG	Metoclopramide	Metoclopramide	TABLET	ORAL	20131230	N/A	ANDA	ANDA072801	Cardinal Health 107, LLC	METOCLOPRAMIDE HYDROCHLORIDE	5 mg/1	10 BLISTER PACK in 1 BAG (55154-4383-0) / 1 TABLET in 1 BLISTER PACK
0093-2204-01	0093-2204	HUMAN PRESCRIPTION DRUG	Metoclopramide	Metoclopramide	TABLET	ORAL	19930701	N/A	ANDA	ANDA072801	Teva Pharmaceuticals USA, Inc.	METOCLOPRAMIDE HYDROCHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE (0093-2204-01)
0093-2204-05	0093-2204	HUMAN PRESCRIPTION DRUG	Metoclopramide	Metoclopramide	TABLET	ORAL	19930701	N/A	ANDA	ANDA072801	Teva Pharmaceuticals USA, Inc.	METOCLOPRAMIDE HYDROCHLORIDE	5 mg/1	500 TABLET in 1 BOTTLE (0093-2204-05)
51079-886-20	51079-886	HUMAN PRESCRIPTION DRUG	Metoclopramide	Metoclopramide	TABLET	ORAL	20131230	N/A	ANDA	ANDA072801	Mylan Institutional Inc.	METOCLOPRAMIDE HYDROCHLORIDE	5 mg/1	100 BLISTER PACK in 1 CARTON (51079-886-20) / 1 TABLET in 1 BLISTER PACK (51079-886-01)
0615-7698-39	0615-7698	HUMAN PRESCRIPTION DRUG	Metoclopramide	Metoclopramide	TABLET	ORAL	20111118	N/A	ANDA	ANDA072801	NCS HealthCare of KY, LLC dba Vangard Labs	METOCLOPRAMIDE HYDROCHLORIDE	5 mg/1	30 TABLET in 1 BLISTER PACK (0615-7698-39)