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
70771-1057-5	70771-1057	HUMAN PRESCRIPTION DRUG	acamprosate calcium	acamprosate calcium	TABLET, DELAYED RELEASE	ORAL	20170601	N/A	ANDA	ANDA205995	Zydus Lifesciences Limited	ACAMPROSATE CALCIUM	333 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE (70771-1057-5)
70771-1057-8	70771-1057	HUMAN PRESCRIPTION DRUG	acamprosate calcium	acamprosate calcium	TABLET, DELAYED RELEASE	ORAL	20170601	N/A	ANDA	ANDA205995	Zydus Lifesciences Limited	ACAMPROSATE CALCIUM	333 mg/1	180 TABLET, DELAYED RELEASE in 1 BOTTLE (70771-1057-8)
70771-1057-9	70771-1057	HUMAN PRESCRIPTION DRUG	acamprosate calcium	acamprosate calcium	TABLET, DELAYED RELEASE	ORAL	20170601	N/A	ANDA	ANDA205995	Zydus Lifesciences Limited	ACAMPROSATE CALCIUM	333 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (70771-1057-9)
68382-569-01	68382-569	HUMAN PRESCRIPTION DRUG	acamprosate calcium	acamprosate calcium	TABLET, DELAYED RELEASE	ORAL	20170601	N/A	ANDA	ANDA205995	Zydus Pharmaceuticals (USA) Inc.	ACAMPROSATE CALCIUM	333 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (68382-569-01)
68382-569-05	68382-569	HUMAN PRESCRIPTION DRUG	acamprosate calcium	acamprosate calcium	TABLET, DELAYED RELEASE	ORAL	20170601	N/A	ANDA	ANDA205995	Zydus Pharmaceuticals (USA) Inc.	ACAMPROSATE CALCIUM	333 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE (68382-569-05)
68382-569-06	68382-569	HUMAN PRESCRIPTION DRUG	acamprosate calcium	acamprosate calcium	TABLET, DELAYED RELEASE	ORAL	20170601	N/A	ANDA	ANDA205995	Zydus Pharmaceuticals (USA) Inc.	ACAMPROSATE CALCIUM	333 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (68382-569-06)
68382-569-10	68382-569	HUMAN PRESCRIPTION DRUG	acamprosate calcium	acamprosate calcium	TABLET, DELAYED RELEASE	ORAL	20170601	N/A	ANDA	ANDA205995	Zydus Pharmaceuticals (USA) Inc.	ACAMPROSATE CALCIUM	333 mg/1	1000 TABLET, DELAYED RELEASE in 1 BOTTLE (68382-569-10)
68382-569-16	68382-569	HUMAN PRESCRIPTION DRUG	acamprosate calcium	acamprosate calcium	TABLET, DELAYED RELEASE	ORAL	20170601	N/A	ANDA	ANDA205995	Zydus Pharmaceuticals (USA) Inc.	ACAMPROSATE CALCIUM	333 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (68382-569-16)
68382-569-28	68382-569	HUMAN PRESCRIPTION DRUG	acamprosate calcium	acamprosate calcium	TABLET, DELAYED RELEASE	ORAL	20170601	N/A	ANDA	ANDA205995	Zydus Pharmaceuticals (USA) Inc.	ACAMPROSATE CALCIUM	333 mg/1	180 TABLET, DELAYED RELEASE in 1 BOTTLE (68382-569-28)
70771-1057-3	70771-1057	HUMAN PRESCRIPTION DRUG	acamprosate calcium	acamprosate calcium	TABLET, DELAYED RELEASE	ORAL	20170601	N/A	ANDA	ANDA205995	Zydus Lifesciences Limited	ACAMPROSATE CALCIUM	333 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (70771-1057-3)
70771-1057-1	70771-1057	HUMAN PRESCRIPTION DRUG	acamprosate calcium	acamprosate calcium	TABLET, DELAYED RELEASE	ORAL	20170601	N/A	ANDA	ANDA205995	Zydus Lifesciences Limited	ACAMPROSATE CALCIUM	333 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (70771-1057-1)
70771-1057-0	70771-1057	HUMAN PRESCRIPTION DRUG	acamprosate calcium	acamprosate calcium	TABLET, DELAYED RELEASE	ORAL	20170601	N/A	ANDA	ANDA205995	Zydus Lifesciences Limited	ACAMPROSATE CALCIUM	333 mg/1	1000 TABLET, DELAYED RELEASE in 1 BOTTLE (70771-1057-0)