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
16571-783-01	16571-783	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20080926	N/A	ANDA	ANDA078643	Rising Pharma Holdings, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16571-783-01)
16571-783-10	16571-783	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20080926	N/A	ANDA	ANDA078643	Rising Pharma Holdings, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (16571-783-10)
16571-783-50	16571-783	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20080926	N/A	ANDA	ANDA078643	Rising Pharma Holdings, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (16571-783-50)
65862-191-01	65862-191	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20080926	N/A	ANDA	ANDA078643	Aurobindo Pharma Limited	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65862-191-01)
65862-191-05	65862-191	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20080926	N/A	ANDA	ANDA078643	Aurobindo Pharma Limited	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65862-191-05)
65862-191-99	65862-191	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20080926	N/A	ANDA	ANDA078643	Aurobindo Pharma Limited	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65862-191-99)
68788-8221-9	68788-8221	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20220909	N/A	ANDA	ANDA078643	Preferred Pharmaceuticals Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68788-8221-9)
68788-8221-2	68788-8221	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20220909	N/A	ANDA	ANDA078643	Preferred Pharmaceuticals Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (68788-8221-2)
68788-8221-3	68788-8221	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20220909	N/A	ANDA	ANDA078643	Preferred Pharmaceuticals Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68788-8221-3)
16571-782-01	16571-782	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20080926	N/A	ANDA	ANDA078643	Rising Pharma Holdings, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16571-782-01)
16571-782-10	16571-782	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20080926	N/A	ANDA	ANDA078643	Rising Pharma Holdings, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (16571-782-10)
16571-782-50	16571-782	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20080926	N/A	ANDA	ANDA078643	Rising Pharma Holdings, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (16571-782-50)
65862-190-01	65862-190	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20080926	N/A	ANDA	ANDA078643	Aurobindo Pharma Limited	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65862-190-01)
65862-190-05	65862-190	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20080926	N/A	ANDA	ANDA078643	Aurobindo Pharma Limited	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65862-190-05)
65862-190-99	65862-190	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20080926	N/A	ANDA	ANDA078643	Aurobindo Pharma Limited	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65862-190-99)
71205-678-30	71205-678	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20220727	N/A	ANDA	ANDA078643	Proficient Rx LP	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71205-678-30)
71205-678-60	71205-678	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20220727	N/A	ANDA	ANDA078643	Proficient Rx LP	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71205-678-60)
71205-678-90	71205-678	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20220727	N/A	ANDA	ANDA078643	Proficient Rx LP	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71205-678-90)
82868-008-30	82868-008	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20240429	N/A	ANDA	ANDA078643	Northwind Health Company, LLC	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82868-008-30)
68788-8167-2	68788-8167	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20220408	N/A	ANDA	ANDA078643	Preferred Pharmaceuticals Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (68788-8167-2)