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
71610-016-92	71610-016	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20171227	N/A	ANDA	ANDA078048	Aphena Pharma Solutions - Tennessee, LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	270 TABLET, FILM COATED in 1 BOTTLE (71610-016-92)
68084-753-25	68084-753	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20160104	N/A	ANDA	ANDA078048	American Health Packaging	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-753-25) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-753-95)
68084-753-65	68084-753	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20240327	N/A	ANDA	ANDA078048	American Health Packaging	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	50 BLISTER PACK in 1 CARTON (68084-753-65) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-753-11)
63187-094-30	63187-094	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20150701	N/A	ANDA	ANDA078048	Proficient Rx LP	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63187-094-30)
63187-094-15	63187-094	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20200113	N/A	ANDA	ANDA078048	Proficient Rx LP	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (63187-094-15)
63187-094-10	63187-094	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20180601	N/A	ANDA	ANDA078048	Proficient Rx LP	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (63187-094-10)
10702-006-01	10702-006	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20140731	N/A	ANDA	ANDA078048	KVK-TECH, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (10702-006-01)
10702-006-10	10702-006	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20140731	N/A	ANDA	ANDA078048	KVK-TECH, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (10702-006-10)
10702-006-50	10702-006	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20140731	N/A	ANDA	ANDA078048	KVK-TECH, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (10702-006-50)
10702-007-01	10702-007	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20140731	N/A	ANDA	ANDA078048	KVK-TECH, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (10702-007-01)
10702-007-03	10702-007	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20140731	N/A	ANDA	ANDA078048	KVK-TECH, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (10702-007-03)
10702-007-09	10702-007	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20181129	N/A	ANDA	ANDA078048	KVK-TECH, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (10702-007-09)
10702-007-10	10702-007	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20140731	N/A	ANDA	ANDA078048	KVK-TECH, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (10702-007-10)
10702-007-50	10702-007	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20140731	N/A	ANDA	ANDA078048	KVK-TECH, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (10702-007-50)