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 49 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
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)
50090-1848-0 50090-1848 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20150528 N/A ANDA ANDA078722 A-S Medication Solutions CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (50090-1848-0)
50090-1848-1 50090-1848 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20150528 N/A ANDA ANDA078722 A-S Medication Solutions CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-1848-1)
50090-1848-2 50090-1848 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20150528 N/A ANDA ANDA078722 A-S Medication Solutions CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (50090-1848-2)
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)
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)
68788-9967-2 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 20 TABLET, FILM COATED in 1 BOTTLE (68788-9967-2)
68788-9967-7 68788-9967 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20190814 N/A ANDA ANDA078722 Preferred Pharmaceuticals, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 8 TABLET, FILM COATED in 1 BOTTLE (68788-9967-7)
68788-9967-3 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 30 TABLET, FILM COATED in 1 BOTTLE (68788-9967-3)
68788-9967-1 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/1 100 TABLET, FILM COATED in 1 BOTTLE (68788-9967-1)
76420-010-01 76420-010 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20221021 N/A ANDA ANDA078722 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76420-010-01)
76420-010-05 76420-010 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20221021 N/A ANDA ANDA078722 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (76420-010-05)
76420-010-12 76420-010 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20230316 N/A ANDA ANDA078722 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (76420-010-12)
76420-010-15 76420-010 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20221021 N/A ANDA ANDA078722 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (76420-010-15)
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