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
76420-877-10	76420-877	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Acetaminophen	Hydrocodone Bitartrate and Acetaminophen	TABLET	ORAL	20241112	N/A	ANDA	ANDA202214	Asclemed USA, Inc.	ACETAMINOPHEN; HYDROCODONE BITARTRATE	325 mg/1; 10 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (76420-877-10)
76420-877-14	76420-877	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Acetaminophen	Hydrocodone Bitartrate and Acetaminophen	TABLET	ORAL	20241112	N/A	ANDA	ANDA202214	Asclemed USA, Inc.	ACETAMINOPHEN; HYDROCODONE BITARTRATE	325 mg/1; 10 mg/1	14 TABLET in 1 BOTTLE, PLASTIC (76420-877-14)
76420-877-20	76420-877	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Acetaminophen	Hydrocodone Bitartrate and Acetaminophen	TABLET	ORAL	20241112	N/A	ANDA	ANDA202214	Asclemed USA, Inc.	ACETAMINOPHEN; HYDROCODONE BITARTRATE	325 mg/1; 10 mg/1	20 TABLET in 1 BOTTLE, PLASTIC (76420-877-20)
76420-877-30	76420-877	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Acetaminophen	Hydrocodone Bitartrate and Acetaminophen	TABLET	ORAL	20241112	N/A	ANDA	ANDA202214	Asclemed USA, Inc.	ACETAMINOPHEN; HYDROCODONE BITARTRATE	325 mg/1; 10 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (76420-877-30)
76420-877-60	76420-877	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Acetaminophen	Hydrocodone Bitartrate and Acetaminophen	TABLET	ORAL	20241112	N/A	ANDA	ANDA202214	Asclemed USA, Inc.	ACETAMINOPHEN; HYDROCODONE BITARTRATE	325 mg/1; 10 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (76420-877-60)
76420-877-90	76420-877	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Acetaminophen	Hydrocodone Bitartrate and Acetaminophen	TABLET	ORAL	20241112	N/A	ANDA	ANDA202214	Asclemed USA, Inc.	ACETAMINOPHEN; HYDROCODONE BITARTRATE	325 mg/1; 10 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (76420-877-90)