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
43063-494-20	43063-494	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20190904	N/A	ANDA	ANDA078048	PD-Rx Pharmaceuticals, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-494-20)
43063-494-30	43063-494	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20140731	N/A	ANDA	ANDA078048	PD-Rx Pharmaceuticals, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-494-30)
43063-494-60	43063-494	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20140731	N/A	ANDA	ANDA078048	PD-Rx Pharmaceuticals, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-494-60)
43063-494-82	43063-494	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20181205	N/A	ANDA	ANDA078048	PD-Rx Pharmaceuticals, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-494-82)
43063-494-90	43063-494	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20140731	N/A	ANDA	ANDA078048	PD-Rx Pharmaceuticals, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-494-90)
43063-494-95	43063-494	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20181204	N/A	ANDA	ANDA078048	PD-Rx Pharmaceuticals, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-494-95)
71610-016-30	71610-016	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20200408	N/A	ANDA	ANDA078048	Aphena Pharma Solutions - Tennessee, LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71610-016-30)
71610-016-45	71610-016	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20171207	N/A	ANDA	ANDA078048	Aphena Pharma Solutions - Tennessee, LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	45 TABLET, FILM COATED in 1 BOTTLE (71610-016-45)
71610-016-53	71610-016	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20200505	N/A	ANDA	ANDA078048	Aphena Pharma Solutions - Tennessee, LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71610-016-53)
71610-016-70	71610-016	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20200505	N/A	ANDA	ANDA078048	Aphena Pharma Solutions - Tennessee, LLC	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71610-016-70)
43063-494-21	43063-494	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20140731	N/A	ANDA	ANDA078048	PD-Rx Pharmaceuticals, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-494-21)
43063-494-14	43063-494	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20140731	N/A	ANDA	ANDA078048	PD-Rx Pharmaceuticals, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-494-14)
43063-494-15	43063-494	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20140731	N/A	ANDA	ANDA078048	PD-Rx Pharmaceuticals, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-494-15)
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)