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
43353-978-92	43353-978	HUMAN PRESCRIPTION DRUG	Oxybutynin Chloride	Oxybutynin Chloride	TABLET	ORAL	20141101	N/A	ANDA	ANDA074625	Aphena Pharma Solutions - Tennessee, LLC	OXYBUTYNIN CHLORIDE	5 mg/1	270 TABLET in 1 BOTTLE (43353-978-92)
0832-0038-00	0832-0038	HUMAN PRESCRIPTION DRUG	Oxybutynin Chloride	Oxybutynin Chloride	TABLET	ORAL	20111107	N/A	ANDA	ANDA074625	Upsher-Smith Laboratories, LLC	OXYBUTYNIN CHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE (0832-0038-00)
0832-0038-01	0832-0038	HUMAN PRESCRIPTION DRUG	Oxybutynin Chloride	Oxybutynin Chloride	TABLET	ORAL	20180315	N/A	ANDA	ANDA074625	Upsher-Smith Laboratories, LLC	OXYBUTYNIN CHLORIDE	5 mg/1	100 BLISTER PACK in 1 CARTON (0832-0038-01) / 1 TABLET in 1 BLISTER PACK (0832-0038-89)
0832-0038-10	0832-0038	HUMAN PRESCRIPTION DRUG	Oxybutynin Chloride	Oxybutynin Chloride	TABLET	ORAL	20111107	N/A	ANDA	ANDA074625	Upsher-Smith Laboratories, LLC	OXYBUTYNIN CHLORIDE	5 mg/1	1000 TABLET in 1 BOTTLE (0832-0038-10)
0832-0038-50	0832-0038	HUMAN PRESCRIPTION DRUG	Oxybutynin Chloride	Oxybutynin Chloride	TABLET	ORAL	20111107	N/A	ANDA	ANDA074625	Upsher-Smith Laboratories, LLC	OXYBUTYNIN CHLORIDE	5 mg/1	500 TABLET in 1 BOTTLE (0832-0038-50)