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
70010-672-01	70010-672	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Acetaminophen	Hydrocodone Bitartrate and Acetaminophen	TABLET	ORAL	20210818	N/A	ANDA	ANDA211729	Granules Pharmaceuticals Inc.	ACETAMINOPHEN; HYDROCODONE BITARTRATE	325 mg/1; 5 mg/1	100 TABLET in 1 BOTTLE (70010-672-01)
70010-672-05	70010-672	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Acetaminophen	Hydrocodone Bitartrate and Acetaminophen	TABLET	ORAL	20210818	N/A	ANDA	ANDA211729	Granules Pharmaceuticals Inc.	ACETAMINOPHEN; HYDROCODONE BITARTRATE	325 mg/1; 5 mg/1	500 TABLET in 1 BOTTLE (70010-672-05)
70010-673-01	70010-673	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Acetaminophen	Hydrocodone Bitartrate and Acetaminophen	TABLET	ORAL	20210818	N/A	ANDA	ANDA211729	Granules Pharmaceuticals Inc.	ACETAMINOPHEN; HYDROCODONE BITARTRATE	325 mg/1; 7.5 mg/1	100 TABLET in 1 BOTTLE (70010-673-01)
70010-673-05	70010-673	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Acetaminophen	Hydrocodone Bitartrate and Acetaminophen	TABLET	ORAL	20210818	N/A	ANDA	ANDA211729	Granules Pharmaceuticals Inc.	ACETAMINOPHEN; HYDROCODONE BITARTRATE	325 mg/1; 7.5 mg/1	500 TABLET in 1 BOTTLE (70010-673-05)
70010-674-01	70010-674	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Acetaminophen	Hydrocodone Bitartrate and Acetaminophen	TABLET	ORAL	20210818	N/A	ANDA	ANDA211729	Granules Pharmaceuticals Inc.	ACETAMINOPHEN; HYDROCODONE BITARTRATE	325 mg/1; 10 mg/1	100 TABLET in 1 BOTTLE (70010-674-01)
70010-674-05	70010-674	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Acetaminophen	Hydrocodone Bitartrate and Acetaminophen	TABLET	ORAL	20210818	N/A	ANDA	ANDA211729	Granules Pharmaceuticals Inc.	ACETAMINOPHEN; HYDROCODONE BITARTRATE	325 mg/1; 10 mg/1	500 TABLET in 1 BOTTLE (70010-674-05)