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
71205-989-60	71205-989	HUMAN PRESCRIPTION DRUG	Cyproheptadine Hydrochloride	Cyproheptadine Hydrochloride	TABLET	ORAL	20200415	N/A	ANDA	ANDA207555	Proficient Rx LP	CYPROHEPTADINE HYDROCHLORIDE	4 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (71205-989-60)
71205-989-64	71205-989	HUMAN PRESCRIPTION DRUG	Cyproheptadine Hydrochloride	Cyproheptadine Hydrochloride	TABLET	ORAL	20200415	N/A	ANDA	ANDA207555	Proficient Rx LP	CYPROHEPTADINE HYDROCHLORIDE	4 mg/1	240 TABLET in 1 BOTTLE, PLASTIC (71205-989-64)
71205-989-30	71205-989	HUMAN PRESCRIPTION DRUG	Cyproheptadine Hydrochloride	Cyproheptadine Hydrochloride	TABLET	ORAL	20200415	N/A	ANDA	ANDA207555	Proficient Rx LP	CYPROHEPTADINE HYDROCHLORIDE	4 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (71205-989-30)
71205-989-11	71205-989	HUMAN PRESCRIPTION DRUG	Cyproheptadine Hydrochloride	Cyproheptadine Hydrochloride	TABLET	ORAL	20200415	N/A	ANDA	ANDA207555	Proficient Rx LP	CYPROHEPTADINE HYDROCHLORIDE	4 mg/1	1000 TABLET in 1 BOTTLE, PLASTIC (71205-989-11)
71205-989-00	71205-989	HUMAN PRESCRIPTION DRUG	Cyproheptadine Hydrochloride	Cyproheptadine Hydrochloride	TABLET	ORAL	20200415	N/A	ANDA	ANDA207555	Proficient Rx LP	CYPROHEPTADINE HYDROCHLORIDE	4 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (71205-989-00)
71205-989-67	71205-989	HUMAN PRESCRIPTION DRUG	Cyproheptadine Hydrochloride	Cyproheptadine Hydrochloride	TABLET	ORAL	20200415	N/A	ANDA	ANDA207555	Proficient Rx LP	CYPROHEPTADINE HYDROCHLORIDE	4 mg/1	270 TABLET in 1 BOTTLE, PLASTIC (71205-989-67)
71205-989-90	71205-989	HUMAN PRESCRIPTION DRUG	Cyproheptadine Hydrochloride	Cyproheptadine Hydrochloride	TABLET	ORAL	20200415	N/A	ANDA	ANDA207555	Proficient Rx LP	CYPROHEPTADINE HYDROCHLORIDE	4 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (71205-989-90)
16571-805-01	16571-805	HUMAN PRESCRIPTION DRUG	Cyproheptadine Hydrochloride	Cyproheptadine Hydrochloride	TABLET	ORAL	20220210	N/A	ANDA	ANDA207555	Rising Pharma Holdings, Inc.	CYPROHEPTADINE HYDROCHLORIDE	4 mg/1	100 TABLET in 1 BOTTLE (16571-805-01)
16571-805-10	16571-805	HUMAN PRESCRIPTION DRUG	Cyproheptadine Hydrochloride	Cyproheptadine Hydrochloride	TABLET	ORAL	20220210	N/A	ANDA	ANDA207555	Rising Pharma Holdings, Inc.	CYPROHEPTADINE HYDROCHLORIDE	4 mg/1	1000 TABLET in 1 BOTTLE (16571-805-10)
71205-989-72	71205-989	HUMAN PRESCRIPTION DRUG	Cyproheptadine Hydrochloride	Cyproheptadine Hydrochloride	TABLET	ORAL	20200415	N/A	ANDA	ANDA207555	Proficient Rx LP	CYPROHEPTADINE HYDROCHLORIDE	4 mg/1	120 TABLET in 1 BOTTLE, PLASTIC (71205-989-72)
71205-989-76	71205-989	HUMAN PRESCRIPTION DRUG	Cyproheptadine Hydrochloride	Cyproheptadine Hydrochloride	TABLET	ORAL	20200415	N/A	ANDA	ANDA207555	Proficient Rx LP	CYPROHEPTADINE HYDROCHLORIDE	4 mg/1	360 TABLET in 1 BOTTLE, PLASTIC (71205-989-76)
71205-989-78	71205-989	HUMAN PRESCRIPTION DRUG	Cyproheptadine Hydrochloride	Cyproheptadine Hydrochloride	TABLET	ORAL	20200415	N/A	ANDA	ANDA207555	Proficient Rx LP	CYPROHEPTADINE HYDROCHLORIDE	4 mg/1	180 TABLET in 1 BOTTLE, PLASTIC (71205-989-78)