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
0378-0277-05	0378-0277	HUMAN PRESCRIPTION DRUG	Chlordiazepoxide and Amitriptyline Hydrochloride	chlordiazepoxide and amitriptyline hydrochloride	TABLET, FILM COATED	ORAL	19861210	N/A	ANDA	ANDA071297	Mylan Pharmaceuticals Inc.	AMITRIPTYLINE HYDROCHLORIDE; CHLORDIAZEPOXIDE	27.98 mg/1; 10 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0277-05)
0378-0277-01	0378-0277	HUMAN PRESCRIPTION DRUG	Chlordiazepoxide and Amitriptyline Hydrochloride	chlordiazepoxide and amitriptyline hydrochloride	TABLET, FILM COATED	ORAL	19861210	N/A	ANDA	ANDA071297	Mylan Pharmaceuticals Inc.	AMITRIPTYLINE HYDROCHLORIDE; CHLORDIAZEPOXIDE	27.98 mg/1; 10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0277-01)
0378-0211-05	0378-0211	HUMAN PRESCRIPTION DRUG	Chlordiazepoxide and Amitriptyline Hydrochloride	chlordiazepoxide and amitriptyline hydrochloride	TABLET, FILM COATED	ORAL	19861210	N/A	ANDA	ANDA071297	Mylan Pharmaceuticals Inc.	AMITRIPTYLINE HYDROCHLORIDE; CHLORDIAZEPOXIDE	14 mg/1; 5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0211-05)
0378-0211-01	0378-0211	HUMAN PRESCRIPTION DRUG	Chlordiazepoxide and Amitriptyline Hydrochloride	chlordiazepoxide and amitriptyline hydrochloride	TABLET, FILM COATED	ORAL	19861210	N/A	ANDA	ANDA071297	Mylan Pharmaceuticals Inc.	AMITRIPTYLINE HYDROCHLORIDE; CHLORDIAZEPOXIDE	14 mg/1; 5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0211-01)