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
68047-752-01	68047-752	HUMAN PRESCRIPTION DRUG	ALLZITAL	butalbital and acetaminophen	TABLET	ORAL	20151204	N/A	ANDA	ANDA203484	Larken Laboratories, Inc.	ACETAMINOPHEN; BUTALBITAL	325 mg/1; 25 mg/1	100 TABLET in 1 BOTTLE (68047-752-01)
68047-752-30	68047-752	HUMAN PRESCRIPTION DRUG	ALLZITAL	butalbital and acetaminophen	TABLET	ORAL	20151204	N/A	ANDA	ANDA203484	Larken Laboratories, Inc.	ACETAMINOPHEN; BUTALBITAL	325 mg/1; 25 mg/1	30 TABLET in 1 BOTTLE (68047-752-30)
68047-753-01	68047-753	HUMAN PRESCRIPTION DRUG	Butalbital and Acetaminophen	butalbital and acetaminophen	TABLET	ORAL	20220718	N/A	ANDA	ANDA203484	Larken Laboratories, Inc.	ACETAMINOPHEN; BUTALBITAL	325 mg/1; 25 mg/1	100 TABLET in 1 BOTTLE (68047-753-01)
68047-753-30	68047-753	HUMAN PRESCRIPTION DRUG	Butalbital and Acetaminophen	butalbital and acetaminophen	TABLET	ORAL	20220718	N/A	ANDA	ANDA203484	Larken Laboratories, Inc.	ACETAMINOPHEN; BUTALBITAL	325 mg/1; 25 mg/1	30 TABLET in 1 BOTTLE (68047-753-30)
68047-721-01	68047-721	HUMAN PRESCRIPTION DRUG	Butalbital And Acetaminophen	butalbital and acetaminophen	TABLET	ORAL	20151204	N/A	ANDA	ANDA203484	Larken Laboratories, Inc.	ACETAMINOPHEN; BUTALBITAL	325 mg/1; 50 mg/1	100 TABLET in 1 BOTTLE (68047-721-01)
68047-721-30	68047-721	HUMAN PRESCRIPTION DRUG	Butalbital And Acetaminophen	butalbital and acetaminophen	TABLET	ORAL	20151204	N/A	ANDA	ANDA203484	Larken Laboratories, Inc.	ACETAMINOPHEN; BUTALBITAL	325 mg/1; 50 mg/1	30 TABLET in 1 BOTTLE (68047-721-30)