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
68462-408-60	68462-408	HUMAN PRESCRIPTION DRUG	propafenone hydrochloride	propafenone hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20170908	N/A	ANDA	ANDA205268	Glenmark Pharmaceuticals Inc., USA	PROPAFENONE HYDROCHLORIDE	225 mg/1	60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68462-408-60)
68462-409-60	68462-409	HUMAN PRESCRIPTION DRUG	propafenone hydrochloride	propafenone hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20170908	N/A	ANDA	ANDA205268	Glenmark Pharmaceuticals Inc., USA	PROPAFENONE HYDROCHLORIDE	325 mg/1	60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68462-409-60)
68462-410-60	68462-410	HUMAN PRESCRIPTION DRUG	propafenone hydrochloride	propafenone hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20170908	N/A	ANDA	ANDA205268	Glenmark Pharmaceuticals Inc., USA	PROPAFENONE HYDROCHLORIDE	425 mg/1	60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68462-410-60)
16714-825-01	16714-825	HUMAN PRESCRIPTION DRUG	propafenone hydrochloride	propafenone hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20180716	N/A	ANDA	ANDA205268	Northstar Rx LLC	PROPAFENONE HYDROCHLORIDE	225 mg/1	60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (16714-825-01)
16714-826-01	16714-826	HUMAN PRESCRIPTION DRUG	propafenone hydrochloride	propafenone hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20180716	N/A	ANDA	ANDA205268	Northstar Rx LLC	PROPAFENONE HYDROCHLORIDE	325 mg/1	60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (16714-826-01)
16714-827-01	16714-827	HUMAN PRESCRIPTION DRUG	propafenone hydrochloride	propafenone hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20180716	N/A	ANDA	ANDA205268	Northstar Rx LLC	PROPAFENONE HYDROCHLORIDE	425 mg/1	60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (16714-827-01)