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
43386-352-05	43386-352	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Acetaminophen	Hydrocodone Bitartrate and Acetaminophen	TABLET	ORAL	20161114	N/A	ANDA	ANDA206142	Lupin Pharmaceuticals,Inc.	ACETAMINOPHEN; HYDROCODONE BITARTRATE	300 mg/1; 7.5 mg/1	500 TABLET in 1 BOTTLE (43386-352-05)
43386-353-01	43386-353	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Acetaminophen	Hydrocodone Bitartrate and Acetaminophen	TABLET	ORAL	20161114	N/A	ANDA	ANDA206142	Lupin Pharmaceuticals,Inc.	ACETAMINOPHEN; HYDROCODONE BITARTRATE	300 mg/1; 10 mg/1	100 TABLET in 1 BOTTLE (43386-353-01)
43386-353-05	43386-353	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Acetaminophen	Hydrocodone Bitartrate and Acetaminophen	TABLET	ORAL	20161114	N/A	ANDA	ANDA206142	Lupin Pharmaceuticals,Inc.	ACETAMINOPHEN; HYDROCODONE BITARTRATE	300 mg/1; 10 mg/1	500 TABLET in 1 BOTTLE (43386-353-05)
43386-352-01	43386-352	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Acetaminophen	Hydrocodone Bitartrate and Acetaminophen	TABLET	ORAL	20161114	N/A	ANDA	ANDA206142	Lupin Pharmaceuticals,Inc.	ACETAMINOPHEN; HYDROCODONE BITARTRATE	300 mg/1; 7.5 mg/1	100 TABLET in 1 BOTTLE (43386-352-01)
43386-351-05	43386-351	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Acetaminophen	Hydrocodone Bitartrate and Acetaminophen	TABLET	ORAL	20161114	N/A	ANDA	ANDA206142	Lupin Pharmaceuticals,Inc.	ACETAMINOPHEN; HYDROCODONE BITARTRATE	300 mg/1; 5 mg/1	500 TABLET in 1 BOTTLE (43386-351-05)
43386-351-01	43386-351	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Acetaminophen	Hydrocodone Bitartrate and Acetaminophen	TABLET	ORAL	20161114	N/A	ANDA	ANDA206142	Lupin Pharmaceuticals,Inc.	ACETAMINOPHEN; HYDROCODONE BITARTRATE	300 mg/1; 5 mg/1	100 TABLET in 1 BOTTLE (43386-351-01)