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
52817-231-10	52817-231	HUMAN PRESCRIPTION DRUG	CHLORZOXAZONE	CHLORZOXAZONE	TABLET	ORAL	20201012	N/A	ANDA	ANDA212053	TruPharma, LLC	CHLORZOXAZONE	750 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (52817-231-10)
52817-230-10	52817-230	HUMAN PRESCRIPTION DRUG	CHLORZOXAZONE	CHLORZOXAZONE	TABLET	ORAL	20201012	N/A	ANDA	ANDA212053	TruPharma, LLC	CHLORZOXAZONE	375 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (52817-230-10)
72319-168-05	72319-168	HUMAN PRESCRIPTION DRUG	CHLORZOXAZONE	CHLORZOXAZONE	TABLET	ORAL	20200916	N/A	ANDA	ANDA212053	i3 Pharmaceuticals, LLC	CHLORZOXAZONE	750 mg/1	500 TABLET in 1 BOTTLE, PLASTIC (72319-168-05)
72319-168-04	72319-168	HUMAN PRESCRIPTION DRUG	CHLORZOXAZONE	CHLORZOXAZONE	TABLET	ORAL	20200916	N/A	ANDA	ANDA212053	i3 Pharmaceuticals, LLC	CHLORZOXAZONE	750 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (72319-168-04)
72319-169-04	72319-169	HUMAN PRESCRIPTION DRUG	CHLORZOXAZONE	CHLORZOXAZONE	TABLET	ORAL	20200916	N/A	ANDA	ANDA212053	i3 Pharmaceuticals, LLC	CHLORZOXAZONE	375 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (72319-169-04)
72319-169-05	72319-169	HUMAN PRESCRIPTION DRUG	CHLORZOXAZONE	CHLORZOXAZONE	TABLET	ORAL	20200916	N/A	ANDA	ANDA212053	i3 Pharmaceuticals, LLC	CHLORZOXAZONE	375 mg/1	500 TABLET in 1 BOTTLE, PLASTIC (72319-169-05)