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
59651-305-01	59651-305	HUMAN PRESCRIPTION DRUG	CHLORZOXAZONE	CHLORZOXAZONE	TABLET	ORAL	20230817	N/A	ANDA	ANDA089853	Aurobindo Pharma Limited	CHLORZOXAZONE	375 mg/1	100 TABLET in 1 BOTTLE (59651-305-01)
71205-711-20	71205-711	HUMAN PRESCRIPTION DRUG	CHLORZOXAZONE	CHLORZOXAZONE	TABLET	ORAL	20250312	N/A	ANDA	ANDA089853	Proficient Rx LP	CHLORZOXAZONE	500 mg/1	20 TABLET in 1 BOTTLE (71205-711-20)
71205-711-30	71205-711	HUMAN PRESCRIPTION DRUG	CHLORZOXAZONE	CHLORZOXAZONE	TABLET	ORAL	20221103	N/A	ANDA	ANDA089853	Proficient Rx LP	CHLORZOXAZONE	500 mg/1	30 TABLET in 1 BOTTLE (71205-711-30)
71205-711-60	71205-711	HUMAN PRESCRIPTION DRUG	CHLORZOXAZONE	CHLORZOXAZONE	TABLET	ORAL	20221103	N/A	ANDA	ANDA089853	Proficient Rx LP	CHLORZOXAZONE	500 mg/1	60 TABLET in 1 BOTTLE (71205-711-60)
71205-711-90	71205-711	HUMAN PRESCRIPTION DRUG	CHLORZOXAZONE	CHLORZOXAZONE	TABLET	ORAL	20221103	N/A	ANDA	ANDA089853	Proficient Rx LP	CHLORZOXAZONE	500 mg/1	90 TABLET in 1 BOTTLE (71205-711-90)
80425-0315-1	80425-0315	HUMAN PRESCRIPTION DRUG	Chlorzoxazone	Chlorzoxazone	TABLET	ORAL	20230410	N/A	ANDA	ANDA089853	Advanced Rx Pharmacy of Tennessee, LLC	CHLORZOXAZONE	500 mg/1	30 TABLET in 1 BOTTLE (80425-0315-1)
80425-0315-2	80425-0315	HUMAN PRESCRIPTION DRUG	Chlorzoxazone	Chlorzoxazone	TABLET	ORAL	20230410	N/A	ANDA	ANDA089853	Advanced Rx Pharmacy of Tennessee, LLC	CHLORZOXAZONE	500 mg/1	60 TABLET in 1 BOTTLE (80425-0315-2)
80425-0315-3	80425-0315	HUMAN PRESCRIPTION DRUG	Chlorzoxazone	Chlorzoxazone	TABLET	ORAL	20230410	N/A	ANDA	ANDA089853	Advanced Rx Pharmacy of Tennessee, LLC	CHLORZOXAZONE	500 mg/1	90 TABLET in 1 BOTTLE (80425-0315-3)