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
71335-2009-1	71335-2009	HUMAN PRESCRIPTION DRUG	CHLORZOXAZONE	CHLORZOXAZONE	TABLET	ORAL	20240403	N/A	ANDA	ANDA089853	Bryant Ranch Prepack	CHLORZOXAZONE	500 mg/1	20 TABLET in 1 BOTTLE (71335-2009-1)
71335-2009-2	71335-2009	HUMAN PRESCRIPTION DRUG	CHLORZOXAZONE	CHLORZOXAZONE	TABLET	ORAL	20240403	N/A	ANDA	ANDA089853	Bryant Ranch Prepack	CHLORZOXAZONE	500 mg/1	30 TABLET in 1 BOTTLE (71335-2009-2)
71335-2009-3	71335-2009	HUMAN PRESCRIPTION DRUG	CHLORZOXAZONE	CHLORZOXAZONE	TABLET	ORAL	20240403	N/A	ANDA	ANDA089853	Bryant Ranch Prepack	CHLORZOXAZONE	500 mg/1	40 TABLET in 1 BOTTLE (71335-2009-3)
71335-2009-4	71335-2009	HUMAN PRESCRIPTION DRUG	CHLORZOXAZONE	CHLORZOXAZONE	TABLET	ORAL	20211203	N/A	ANDA	ANDA089853	Bryant Ranch Prepack	CHLORZOXAZONE	500 mg/1	90 TABLET in 1 BOTTLE (71335-2009-4)
71335-2009-5	71335-2009	HUMAN PRESCRIPTION DRUG	CHLORZOXAZONE	CHLORZOXAZONE	TABLET	ORAL	20221222	N/A	ANDA	ANDA089853	Bryant Ranch Prepack	CHLORZOXAZONE	500 mg/1	60 TABLET in 1 BOTTLE (71335-2009-5)
71335-2009-6	71335-2009	HUMAN PRESCRIPTION DRUG	CHLORZOXAZONE	CHLORZOXAZONE	TABLET	ORAL	20240403	N/A	ANDA	ANDA089853	Bryant Ranch Prepack	CHLORZOXAZONE	500 mg/1	100 TABLET in 1 BOTTLE (71335-2009-6)
71335-2009-7	71335-2009	HUMAN PRESCRIPTION DRUG	CHLORZOXAZONE	CHLORZOXAZONE	TABLET	ORAL	20240403	N/A	ANDA	ANDA089853	Bryant Ranch Prepack	CHLORZOXAZONE	500 mg/1	14 TABLET in 1 BOTTLE (71335-2009-7)
71335-2009-8	71335-2009	HUMAN PRESCRIPTION DRUG	CHLORZOXAZONE	CHLORZOXAZONE	TABLET	ORAL	20240403	N/A	ANDA	ANDA089853	Bryant Ranch Prepack	CHLORZOXAZONE	500 mg/1	7 TABLET in 1 BOTTLE (71335-2009-8)
71335-2009-9	71335-2009	HUMAN PRESCRIPTION DRUG	CHLORZOXAZONE	CHLORZOXAZONE	TABLET	ORAL	20240403	N/A	ANDA	ANDA089853	Bryant Ranch Prepack	CHLORZOXAZONE	500 mg/1	120 TABLET in 1 BOTTLE (71335-2009-9)