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
69452-323-20	69452-323	HUMAN PRESCRIPTION DRUG	Cimetidine	cimetidine	TABLET, FILM COATED	ORAL	20250301	N/A	ANDA	ANDA218220	Bionpharma Inc.	CIMETIDINE	200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (69452-323-20)
69452-323-30	69452-323	HUMAN PRESCRIPTION DRUG	Cimetidine	cimetidine	TABLET, FILM COATED	ORAL	20250301	N/A	ANDA	ANDA218220	Bionpharma Inc.	CIMETIDINE	200 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (69452-323-30)
69452-324-20	69452-324	HUMAN PRESCRIPTION DRUG	Cimetidine	cimetidine	TABLET, FILM COATED	ORAL	20250301	N/A	ANDA	ANDA218220	Bionpharma Inc.	CIMETIDINE	300 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (69452-324-20)
69452-324-30	69452-324	HUMAN PRESCRIPTION DRUG	Cimetidine	cimetidine	TABLET, FILM COATED	ORAL	20250301	N/A	ANDA	ANDA218220	Bionpharma Inc.	CIMETIDINE	300 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (69452-324-30)
69452-326-20	69452-326	HUMAN PRESCRIPTION DRUG	Cimetidine	cimetidine	TABLET, FILM COATED	ORAL	20250301	N/A	ANDA	ANDA218220	Bionpharma Inc.	CIMETIDINE	800 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (69452-326-20)
69452-326-30	69452-326	HUMAN PRESCRIPTION DRUG	Cimetidine	cimetidine	TABLET, FILM COATED	ORAL	20250301	N/A	ANDA	ANDA218220	Bionpharma Inc.	CIMETIDINE	800 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (69452-326-30)
69452-325-20	69452-325	HUMAN PRESCRIPTION DRUG	Cimetidine	cimetidine	TABLET, FILM COATED	ORAL	20250301	N/A	ANDA	ANDA218220	Bionpharma Inc.	CIMETIDINE	400 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (69452-325-20)
69452-325-30	69452-325	HUMAN PRESCRIPTION DRUG	Cimetidine	cimetidine	TABLET, FILM COATED	ORAL	20250301	N/A	ANDA	ANDA218220	Bionpharma Inc.	CIMETIDINE	400 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (69452-325-30)