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
43386-480-24	43386-480	HUMAN PRESCRIPTION DRUG	ORPHENADRINE CITRATE	ORPHENADRINE CITRATE	TABLET, EXTENDED RELEASE	ORAL	19980619	N/A	ANDA	ANDA040284	Lupin Pharmaceuticals, Inc.	ORPHENADRINE CITRATE	100 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (43386-480-24)
43386-480-26	43386-480	HUMAN PRESCRIPTION DRUG	ORPHENADRINE CITRATE	ORPHENADRINE CITRATE	TABLET, EXTENDED RELEASE	ORAL	19980619	N/A	ANDA	ANDA040284	Lupin Pharmaceuticals, Inc.	ORPHENADRINE CITRATE	100 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (43386-480-26)
43386-480-28	43386-480	HUMAN PRESCRIPTION DRUG	ORPHENADRINE CITRATE	ORPHENADRINE CITRATE	TABLET, EXTENDED RELEASE	ORAL	19980619	N/A	ANDA	ANDA040284	Lupin Pharmaceuticals, Inc.	ORPHENADRINE CITRATE	100 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (43386-480-28)
82868-040-14	82868-040	HUMAN PRESCRIPTION DRUG	ORPHENADRINE CITRATE	ORPHENADRINE CITRATE	TABLET, EXTENDED RELEASE	ORAL	20240130	N/A	ANDA	ANDA040284	Northwind Health Company, LLC	ORPHENADRINE CITRATE	100 mg/1	14 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82868-040-14)
49999-046-60	49999-046	HUMAN PRESCRIPTION DRUG	Orphenadrine Citrate	Orphenadrine Citrate	TABLET, EXTENDED RELEASE	ORAL	20110207	20261130	ANDA	ANDA040284	Lake Erie Medical DBA Quality Care Products LLC	ORPHENADRINE CITRATE	100 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (49999-046-60)