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）
检索条件:" 注册申请号=ANDA078722"
符合检索条件的记录共 51 条，共 3 页，当前第 2 页 ，可点击列名称排序
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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
68788-9967-6 68788-9967 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20150501 N/A ANDA ANDA078722 Preferred Pharmaceuticals, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-9967-6)
69420-1001-1 69420-1001 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20150325 N/A ANDA ANDA078722 SA3, LLC CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (69420-1001-1)
69420-1001-2 69420-1001 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20150325 N/A ANDA ANDA078722 SA3, LLC CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (69420-1001-2)
69420-1001-3 69420-1001 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20150325 N/A ANDA ANDA078722 SA3, LLC CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (69420-1001-3)
71335-0096-1 71335-0096 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20180320 N/A ANDA ANDA078722 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-0096-1)
71335-0096-4 71335-0096 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20180509 N/A ANDA ANDA078722 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71335-0096-4)
71335-0096-5 71335-0096 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20190927 N/A ANDA ANDA078722 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (71335-0096-5)
71335-0096-6 71335-0096 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20220309 N/A ANDA ANDA078722 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 45 TABLET, FILM COATED in 1 BOTTLE (71335-0096-6)
71335-0096-7 71335-0096 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20180904 N/A ANDA ANDA078722 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 9 TABLET, FILM COATED in 1 BOTTLE (71335-0096-7)
71335-0096-8 71335-0096 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20220309 N/A ANDA ANDA078722 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (71335-0096-8)
71335-0096-9 71335-0096 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20180423 N/A ANDA ANDA078722 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (71335-0096-9)
71335-0096-2 71335-0096 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20180305 N/A ANDA ANDA078722 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-0096-2)
71335-0096-3 71335-0096 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20180320 N/A ANDA ANDA078722 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-0096-3)
71335-0096-0 71335-0096 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20220309 N/A ANDA ANDA078722 Bryant Ranch Prepack CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (71335-0096-0)
80425-0078-1 80425-0078 HUMAN PRESCRIPTION DRUG Cyclobenzaprine HCL Cyclobenzaprine HCL TABLET, FILM COATED ORAL 20150325 N/A ANDA ANDA078722 Advanced Rx of Tennessee, LLC CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (80425-0078-1)
80425-0078-2 80425-0078 HUMAN PRESCRIPTION DRUG Cyclobenzaprine HCL Cyclobenzaprine HCL TABLET, FILM COATED ORAL 20150325 N/A ANDA ANDA078722 Advanced Rx of Tennessee, LLC CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (80425-0078-2)
80425-0078-3 80425-0078 HUMAN PRESCRIPTION DRUG Cyclobenzaprine HCL Cyclobenzaprine HCL TABLET, FILM COATED ORAL 20150325 N/A ANDA ANDA078722 Advanced Rx of Tennessee, LLC CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (80425-0078-3)
80425-0078-4 80425-0078 HUMAN PRESCRIPTION DRUG Cyclobenzaprine HCL Cyclobenzaprine HCL TABLET, FILM COATED ORAL 20150325 N/A ANDA ANDA078722 Advanced Rx of Tennessee, LLC CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (80425-0078-4)
55700-239-30 55700-239 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20150424 20251231 ANDA ANDA078722 Quality Care Products LLC CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (55700-239-30)
85509-1001-3 85509-1001 HUMAN PRESCRIPTION DRUG Cyclobenzaprine HCL Cyclobenzaprine HCL TABLET, FILM COATED ORAL 20250721 N/A ANDA ANDA078722 PHOENIX RX LLC CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (85509-1001-3)
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