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=ANDA090778"
符合检索条件的记录共 37 条，共 2 页，当前第 1 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
63187-612-60 63187-612 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20181201 N/A ANDA ANDA090778 Proficient Rx LP DULOXETINE HYDROCHLORIDE 30 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-612-60)
63187-612-90 63187-612 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20181201 N/A ANDA ANDA090778 Proficient Rx LP DULOXETINE HYDROCHLORIDE 30 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-612-90)
63187-612-30 63187-612 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20181201 N/A ANDA ANDA090778 Proficient Rx LP DULOXETINE HYDROCHLORIDE 30 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-612-30)
63187-666-90 63187-666 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20181201 N/A ANDA ANDA090778 Proficient Rx LP DULOXETINE HYDROCHLORIDE 60 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-666-90)
71610-402-60 71610-402 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20200226 N/A ANDA ANDA090778 Aphena Pharma Solutions - Tennessee, LLC DULOXETINE HYDROCHLORIDE 30 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-402-60)
63187-666-60 63187-666 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20181201 N/A ANDA ANDA090778 Proficient Rx LP DULOXETINE HYDROCHLORIDE 60 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-666-60)
63187-666-30 63187-666 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20181201 N/A ANDA ANDA090778 Proficient Rx LP DULOXETINE HYDROCHLORIDE 60 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-666-30)
71610-401-83 71610-401 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20200226 N/A ANDA ANDA090778 Aphena Pharma Solutions - Tennessee, LLC DULOXETINE HYDROCHLORIDE 20 mg/1 3600 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-401-83)
0904-7043-04 0904-7043 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20131211 20260331 ANDA ANDA090778 Major Pharmaceuticals DULOXETINE HYDROCHLORIDE 20 mg/1 30 BLISTER PACK in 1 CARTON (0904-7043-04) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
0904-7044-61 0904-7044 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20131211 20260430 ANDA ANDA090778 Major Pharmaceuticals DULOXETINE HYDROCHLORIDE 30 mg/1 100 BLISTER PACK in 1 CARTON (0904-7044-61) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
0904-7045-61 0904-7045 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20131211 20260430 ANDA ANDA090778 Major Pharmaceuticals DULOXETINE HYDROCHLORIDE 60 mg/1 100 BLISTER PACK in 1 CARTON (0904-7045-61) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
80425-0013-2 80425-0013 HUMAN PRESCRIPTION DRUG Duloxetine HCL DR Duloxetine HCL CAPSULE, DELAYED RELEASE ORAL 20190930 N/A ANDA ANDA090778 Advanced Rx of Tennessee, LLC DULOXETINE HYDROCHLORIDE 30 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0013-2)
80425-0014-1 80425-0014 HUMAN PRESCRIPTION DRUG Duloxetine HCL DR Duloxetine HCL CAPSULE, DELAYED RELEASE ORAL 20221211 N/A ANDA ANDA090778 Advanced Rx of Tennessee, LLC DULOXETINE HYDROCHLORIDE 30 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0014-1)
80425-0014-2 80425-0014 HUMAN PRESCRIPTION DRUG Duloxetine HCL DR Duloxetine HCL CAPSULE, DELAYED RELEASE ORAL 20221211 N/A ANDA ANDA090778 Advanced Rx of Tennessee, LLC DULOXETINE HYDROCHLORIDE 30 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0014-2)
80425-0013-1 80425-0013 HUMAN PRESCRIPTION DRUG Duloxetine HCL DR Duloxetine HCL CAPSULE, DELAYED RELEASE ORAL 20190930 N/A ANDA ANDA090778 Advanced Rx of Tennessee, LLC DULOXETINE HYDROCHLORIDE 30 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0013-1)
57237-017-60 57237-017 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20131211 20260430 ANDA ANDA090778 Rising Pharma Holdings, Inc. DULOXETINE HYDROCHLORIDE 20 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-017-60)
57237-019-99 57237-019 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20131211 20260331 ANDA ANDA090778 Rising Pharma Holdings, Inc. DULOXETINE HYDROCHLORIDE 60 mg/1 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (57237-019-99)
60687-734-01 60687-734 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20230403 20260331 ANDA ANDA090778 American Health Packaging DULOXETINE HYDROCHLORIDE 30 mg/1 100 BLISTER PACK in 1 CARTON (60687-734-01) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (60687-734-11)
60687-723-21 60687-723 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20230425 20260531 ANDA ANDA090778 American Health Packaging DULOXETINE HYDROCHLORIDE 20 mg/1 30 BLISTER PACK in 1 CARTON (60687-723-21) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (60687-723-11)
55154-2341-0 55154-2341 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20131211 20260430 ANDA ANDA090778 Cardinal Health 107, LLC DULOXETINE HYDROCHLORIDE 60 mg/1 10 BLISTER PACK in 1 BAG (55154-2341-0) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
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