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
42571-302-01	42571-302	HUMAN PRESCRIPTION DRUG	Chlordiazepoxide and Amitriptyline Hydrochloride	Chlordiazepoxide and Amitriptyline Hydrochloride	TABLET	ORAL	20220401	N/A	ANDA	ANDA211925	Micro Labs Limited	AMITRIPTYLINE HYDROCHLORIDE; CHLORDIAZEPOXIDE	5 mg/1; 12.5 mg/1	100 TABLET in 1 BOTTLE (42571-302-01)
42571-302-05	42571-302	HUMAN PRESCRIPTION DRUG	Chlordiazepoxide and Amitriptyline Hydrochloride	Chlordiazepoxide and Amitriptyline Hydrochloride	TABLET	ORAL	20220401	N/A	ANDA	ANDA211925	Micro Labs Limited	AMITRIPTYLINE HYDROCHLORIDE; CHLORDIAZEPOXIDE	5 mg/1; 12.5 mg/1	500 TABLET in 1 BOTTLE (42571-302-05)
42571-303-01	42571-303	HUMAN PRESCRIPTION DRUG	Chlordiazepoxide and Amitriptyline Hydrochloride	Chlordiazepoxide and Amitriptyline Hydrochloride	TABLET	ORAL	20220401	N/A	ANDA	ANDA211925	Micro Labs Limited	AMITRIPTYLINE HYDROCHLORIDE; CHLORDIAZEPOXIDE	10 mg/1; 25 mg/1	100 TABLET in 1 BOTTLE (42571-303-01)
42571-303-05	42571-303	HUMAN PRESCRIPTION DRUG	Chlordiazepoxide and Amitriptyline Hydrochloride	Chlordiazepoxide and Amitriptyline Hydrochloride	TABLET	ORAL	20220401	N/A	ANDA	ANDA211925	Micro Labs Limited	AMITRIPTYLINE HYDROCHLORIDE; CHLORDIAZEPOXIDE	10 mg/1; 25 mg/1	500 TABLET in 1 BOTTLE (42571-303-05)