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=ANDA213324"
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
76420-841-90 76420-841 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20240816 N/A ANDA ANDA213324 Asclemed USA, Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (76420-841-90)
29300-413-01 29300-413 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20200930 N/A ANDA ANDA213324 Unichem Pharmaceuticals (USA), Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (29300-413-01)
29300-413-05 29300-413 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20200930 N/A ANDA ANDA213324 Unichem Pharmaceuticals (USA), Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (29300-413-05)
29300-413-10 29300-413 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20200930 N/A ANDA ANDA213324 Unichem Pharmaceuticals (USA), Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (29300-413-10)
29300-413-19 29300-413 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20211118 N/A ANDA ANDA213324 Unichem Pharmaceuticals (USA), Inc. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (29300-413-19)
29300-414-01 29300-414 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20200930 N/A ANDA ANDA213324 Unichem Pharmaceuticals (USA), Inc. CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (29300-414-01)
29300-414-10 29300-414 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20200930 N/A ANDA ANDA213324 Unichem Pharmaceuticals (USA), Inc. CYCLOBENZAPRINE HYDROCHLORIDE 7.5 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (29300-414-10)
29300-415-01 29300-415 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20200930 N/A ANDA ANDA213324 Unichem Pharmaceuticals (USA), Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (29300-415-01)
29300-415-05 29300-415 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20200930 N/A ANDA ANDA213324 Unichem Pharmaceuticals (USA), Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (29300-415-05)
29300-415-10 29300-415 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20200930 N/A ANDA ANDA213324 Unichem Pharmaceuticals (USA), Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (29300-415-10)
29300-415-19 29300-415 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20211118 N/A ANDA ANDA213324 Unichem Pharmaceuticals (USA), Inc. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (29300-415-19)
70518-3702-1 70518-3702 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20230412 N/A ANDA ANDA213324 REMEDYREPACK INC. CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3702-1)
80425-0155-1 80425-0155 HUMAN PRESCRIPTION DRUG Cyclobenzaprine HCL Cyclobenzaprine HCL TABLET, FILM COATED ORAL 20230330 N/A ANDA ANDA213324 Advanced Rx Pharmacy of Tennessee, LLC CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (80425-0155-1)
80425-0155-2 80425-0155 HUMAN PRESCRIPTION DRUG Cyclobenzaprine HCL Cyclobenzaprine HCL TABLET, FILM COATED ORAL 20230330 N/A ANDA ANDA213324 Advanced Rx Pharmacy of Tennessee, LLC CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (80425-0155-2)
80425-0155-3 80425-0155 HUMAN PRESCRIPTION DRUG Cyclobenzaprine HCL Cyclobenzaprine HCL TABLET, FILM COATED ORAL 20230330 N/A ANDA ANDA213324 Advanced Rx Pharmacy of Tennessee, LLC CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (80425-0155-3)
80425-0155-4 80425-0155 HUMAN PRESCRIPTION DRUG Cyclobenzaprine HCL Cyclobenzaprine HCL TABLET, FILM COATED ORAL 20230330 N/A ANDA ANDA213324 Advanced Rx Pharmacy of Tennessee, LLC CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (80425-0155-4)
80425-0155-5 80425-0155 HUMAN PRESCRIPTION DRUG Cyclobenzaprine HCL Cyclobenzaprine HCL TABLET, FILM COATED ORAL 20230330 N/A ANDA ANDA213324 Advanced Rx Pharmacy of Tennessee, LLC CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (80425-0155-5)
85509-1415-3 85509-1415 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20251114 N/A ANDA ANDA213324 PHOENIX RX LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (85509-1415-3)
85509-1415-6 85509-1415 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20251114 N/A ANDA ANDA213324 PHOENIX RX LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (85509-1415-6)
85509-1415-9 85509-1415 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20251114 N/A ANDA ANDA213324 PHOENIX RX LLC CYCLOBENZAPRINE HYDROCHLORIDE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (85509-1415-9)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase