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
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)
68788-9967-3 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)
68788-9967-6 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)
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)
68788-9967-8 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/1 120 TABLET, FILM COATED in 1 BOTTLE (68788-9967-8)
68788-9967-9 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 90 TABLET, FILM COATED in 1 BOTTLE (68788-9967-9)
63187-590-14 63187-590 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20240904 N/A ANDA ANDA078722 Proficient Rx LP CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (63187-590-14)
63187-590-20 63187-590 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20181201 N/A ANDA ANDA078722 Proficient Rx LP CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (63187-590-20)
63187-590-30 63187-590 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20181201 N/A ANDA ANDA078722 Proficient Rx LP CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (63187-590-30)
63187-590-60 63187-590 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20181201 N/A ANDA ANDA078722 Proficient Rx LP CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (63187-590-60)
63187-590-72 63187-590 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20181201 N/A ANDA ANDA078722 Proficient Rx LP CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (63187-590-72)
63187-590-90 63187-590 HUMAN PRESCRIPTION DRUG Cyclobenzaprine Hydrochloride Cyclobenzaprine Hydrochloride TABLET, FILM COATED ORAL 20181201 N/A ANDA ANDA078722 Proficient Rx LP CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (63187-590-90)
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)
85509-1001-1 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/1 120 TABLET, FILM COATED in 1 BOTTLE (85509-1001-1)
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)
85509-1001-6 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 60 TABLET, FILM COATED in 1 BOTTLE (85509-1001-6)
85509-1001-9 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 90 TABLET, FILM COATED in 1 BOTTLE (85509-1001-9)
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)
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