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
0093-3422-05	0093-3422	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20210720	N/A	ANDA	ANDA071611	Teva Pharmaceuticals USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (0093-3422-05)
0093-3422-10	0093-3422	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20210720	N/A	ANDA	ANDA071611	Teva Pharmaceuticals USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (0093-3422-10)
0093-3422-01	0093-3422	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20210720	N/A	ANDA	ANDA071611	Teva Pharmaceuticals USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0093-3422-01)
0093-3421-01	0093-3421	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20210720	N/A	ANDA	ANDA071611	Teva Pharmaceuticals USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0093-3421-01)
0093-3420-01	0093-3420	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20210720	N/A	ANDA	ANDA071611	Teva Pharmaceuticals USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0093-3420-01)
68071-3627-5	68071-3627	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20240613	N/A	ANDA	ANDA071611	NuCare Pharmaceuticals,Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (68071-3627-5)
68071-3627-7	68071-3627	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20240613	N/A	ANDA	ANDA071611	NuCare Pharmaceuticals,Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	10 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (68071-3627-7)
76420-268-07	76420-268	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20220903	N/A	ANDA	ANDA071611	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	7 TABLET, FILM COATED in 1 BOTTLE (76420-268-07)
76420-268-15	76420-268	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20220903	N/A	ANDA	ANDA071611	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (76420-268-15)
76420-268-20	76420-268	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20220903	N/A	ANDA	ANDA071611	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (76420-268-20)
76420-268-30	76420-268	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20220903	N/A	ANDA	ANDA071611	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76420-268-30)
76420-268-60	76420-268	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20220903	N/A	ANDA	ANDA071611	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (76420-268-60)
76420-268-90	76420-268	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20220903	N/A	ANDA	ANDA071611	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (76420-268-90)
76420-269-01	76420-269	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20220903	N/A	ANDA	ANDA071611	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	1 TABLET, FILM COATED in 1 BOTTLE (76420-269-01)
76420-268-10	76420-268	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20220903	N/A	ANDA	ANDA071611	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (76420-268-10)
76420-268-01	76420-268	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20220903	N/A	ANDA	ANDA071611	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	1 TABLET, FILM COATED in 1 BOTTLE (76420-268-01)
76420-268-02	76420-268	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20220903	N/A	ANDA	ANDA071611	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	2 TABLET, FILM COATED in 1 BOTTLE (76420-268-02)
76420-269-02	76420-269	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20220903	N/A	ANDA	ANDA071611	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	2 TABLET, FILM COATED in 1 BOTTLE (76420-269-02)
76420-269-20	76420-269	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20220903	N/A	ANDA	ANDA071611	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (76420-269-20)
76420-269-30	76420-269	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20220903	N/A	ANDA	ANDA071611	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76420-269-30)