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
72603-112-01	72603-112	HUMAN PRESCRIPTION DRUG	Clorazepate Dipotassium	Clorazepate Dipotassium	TABLET	ORAL	20221024	N/A	ANDA	ANDA075731	NORTHSTAR RX LLC	CLORAZEPATE DIPOTASSIUM	3.75 mg/1	100 TABLET in 1 BOTTLE (72603-112-01)
72603-112-02	72603-112	HUMAN PRESCRIPTION DRUG	Clorazepate Dipotassium	Clorazepate Dipotassium	TABLET	ORAL	20221024	N/A	ANDA	ANDA075731	NORTHSTAR RX LLC	CLORAZEPATE DIPOTASSIUM	3.75 mg/1	500 TABLET in 1 BOTTLE (72603-112-02)
72603-113-02	72603-113	HUMAN PRESCRIPTION DRUG	Clorazepate Dipotassium	Clorazepate Dipotassium	TABLET	ORAL	20221024	N/A	ANDA	ANDA075731	NORTHSTAR RX LLC	CLORAZEPATE DIPOTASSIUM	7.5 mg/1	500 TABLET in 1 BOTTLE (72603-113-02)
72603-113-01	72603-113	HUMAN PRESCRIPTION DRUG	Clorazepate Dipotassium	Clorazepate Dipotassium	TABLET	ORAL	20221024	N/A	ANDA	ANDA075731	NORTHSTAR RX LLC	CLORAZEPATE DIPOTASSIUM	7.5 mg/1	100 TABLET in 1 BOTTLE (72603-113-01)
72603-114-01	72603-114	HUMAN PRESCRIPTION DRUG	Clorazepate Dipotassium	Clorazepate Dipotassium	TABLET	ORAL	20221024	N/A	ANDA	ANDA075731	NORTHSTAR RX LLC	CLORAZEPATE DIPOTASSIUM	15 mg/1	100 TABLET in 1 BOTTLE (72603-114-01)
51672-4043-1	51672-4043	HUMAN PRESCRIPTION DRUG	Clorazepate Dipotassium	Clorazepate Dipotassium	TABLET	ORAL	20000427	N/A	ANDA	ANDA075731	Taro Pharmaceuticals U.S.A., Inc.	CLORAZEPATE DIPOTASSIUM	7.5 mg/1	100 TABLET in 1 BOTTLE (51672-4043-1)
51672-4043-2	51672-4043	HUMAN PRESCRIPTION DRUG	Clorazepate Dipotassium	Clorazepate Dipotassium	TABLET	ORAL	20000427	N/A	ANDA	ANDA075731	Taro Pharmaceuticals U.S.A., Inc.	CLORAZEPATE DIPOTASSIUM	7.5 mg/1	500 TABLET in 1 BOTTLE (51672-4043-2)
51672-4043-3	51672-4043	HUMAN PRESCRIPTION DRUG	Clorazepate Dipotassium	Clorazepate Dipotassium	TABLET	ORAL	20000427	N/A	ANDA	ANDA075731	Taro Pharmaceuticals U.S.A., Inc.	CLORAZEPATE DIPOTASSIUM	7.5 mg/1	1000 TABLET in 1 BOTTLE (51672-4043-3)
51672-4044-1	51672-4044	HUMAN PRESCRIPTION DRUG	Clorazepate Dipotassium	Clorazepate Dipotassium	TABLET	ORAL	20000427	N/A	ANDA	ANDA075731	Taro Pharmaceuticals U.S.A., Inc.	CLORAZEPATE DIPOTASSIUM	15 mg/1	100 TABLET in 1 BOTTLE (51672-4044-1)
51672-4044-2	51672-4044	HUMAN PRESCRIPTION DRUG	Clorazepate Dipotassium	Clorazepate Dipotassium	TABLET	ORAL	20000427	N/A	ANDA	ANDA075731	Taro Pharmaceuticals U.S.A., Inc.	CLORAZEPATE DIPOTASSIUM	15 mg/1	500 TABLET in 1 BOTTLE (51672-4044-2)
51672-4044-3	51672-4044	HUMAN PRESCRIPTION DRUG	Clorazepate Dipotassium	Clorazepate Dipotassium	TABLET	ORAL	20000427	N/A	ANDA	ANDA075731	Taro Pharmaceuticals U.S.A., Inc.	CLORAZEPATE DIPOTASSIUM	15 mg/1	1000 TABLET in 1 BOTTLE (51672-4044-3)
51672-4042-1	51672-4042	HUMAN PRESCRIPTION DRUG	Clorazepate Dipotassium	Clorazepate Dipotassium	TABLET	ORAL	20000427	N/A	ANDA	ANDA075731	Taro Pharmaceuticals U.S.A., Inc.	CLORAZEPATE DIPOTASSIUM	3.75 mg/1	100 TABLET in 1 BOTTLE (51672-4042-1)
51672-4042-2	51672-4042	HUMAN PRESCRIPTION DRUG	Clorazepate Dipotassium	Clorazepate Dipotassium	TABLET	ORAL	20000427	N/A	ANDA	ANDA075731	Taro Pharmaceuticals U.S.A., Inc.	CLORAZEPATE DIPOTASSIUM	3.75 mg/1	500 TABLET in 1 BOTTLE (51672-4042-2)
51672-4042-3	51672-4042	HUMAN PRESCRIPTION DRUG	Clorazepate Dipotassium	Clorazepate Dipotassium	TABLET	ORAL	20000427	N/A	ANDA	ANDA075731	Taro Pharmaceuticals U.S.A., Inc.	CLORAZEPATE DIPOTASSIUM	3.75 mg/1	1000 TABLET in 1 BOTTLE (51672-4042-3)
43063-893-06	43063-893	HUMAN PRESCRIPTION DRUG	Clorazepate Dipotassium	Clorazepate Dipotassium	TABLET	ORAL	20180912	N/A	ANDA	ANDA075731	PD-Rx Pharmaceuticals, Inc.	CLORAZEPATE DIPOTASSIUM	15 mg/1	6 TABLET in 1 BOTTLE, PLASTIC (43063-893-06)
72789-256-06	72789-256	HUMAN PRESCRIPTION DRUG	Clorazepate Dipotassium	Clorazepate Dipotassium	TABLET	ORAL	20220701	N/A	ANDA	ANDA075731	PD-Rx Pharmaceuticals, Inc.	CLORAZEPATE DIPOTASSIUM	15 mg/1	6 TABLET in 1 BOTTLE, PLASTIC (72789-256-06)