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"
符合检索条件的记录共 125 条，共 7 页，当前第 6 页 ，可点击列名称排序
首页 上一页 下一页 最后一页
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
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)
70518-3251-2 70518-3251 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20211123 N/A ANDA ANDA213324 REMEDYREPACK INC. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3251-2)
70518-3251-5 70518-3251 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20230228 N/A ANDA ANDA213324 REMEDYREPACK INC. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3251-5)
70518-3251-6 70518-3251 HUMAN PRESCRIPTION DRUG Cyclobenzaprine hydrochloride Cyclobenzaprine hydrochloride TABLET, FILM COATED ORAL 20250609 N/A ANDA ANDA213324 REMEDYREPACK INC. CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3251-6)
72189-280-15 72189-280 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE CYCLOBENZAPRINE HYDROCHLORIDE TABLET, FILM COATED ORAL 20211007 N/A ANDA ANDA213324 DirectRx CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (72189-280-15)
72189-280-20 72189-280 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE CYCLOBENZAPRINE HYDROCHLORIDE TABLET, FILM COATED ORAL 20211007 N/A ANDA ANDA213324 DirectRx CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (72189-280-20)
72189-280-30 72189-280 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE CYCLOBENZAPRINE HYDROCHLORIDE TABLET, FILM COATED ORAL 20211007 N/A ANDA ANDA213324 DirectRx CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (72189-280-30)
72189-280-60 72189-280 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE CYCLOBENZAPRINE HYDROCHLORIDE TABLET, FILM COATED ORAL 20211007 N/A ANDA ANDA213324 DirectRx CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (72189-280-60)
72189-280-82 72189-280 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE CYCLOBENZAPRINE HYDROCHLORIDE TABLET, FILM COATED ORAL 20211007 N/A ANDA ANDA213324 DirectRx CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (72189-280-82)
72189-280-90 72189-280 HUMAN PRESCRIPTION DRUG CYCLOBENZAPRINE HYDROCHLORIDE CYCLOBENZAPRINE HYDROCHLORIDE TABLET, FILM COATED ORAL 20211007 N/A ANDA ANDA213324 DirectRx CYCLOBENZAPRINE HYDROCHLORIDE 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (72189-280-90)
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)
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