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"
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
70518-0937-3 70518-0937 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20220906 N/A ANDA ANDA090778 REMEDYREPACK INC. DULOXETINE HYDROCHLORIDE 60 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-0937-3)
70518-0937-4 70518-0937 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20220906 N/A ANDA ANDA090778 REMEDYREPACK INC. DULOXETINE HYDROCHLORIDE 60 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (70518-0937-4)
70518-0937-5 70518-0937 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20221128 N/A ANDA ANDA090778 REMEDYREPACK INC. DULOXETINE HYDROCHLORIDE 60 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-0937-5)
70518-0937-6 70518-0937 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20221128 N/A ANDA ANDA090778 REMEDYREPACK INC. DULOXETINE HYDROCHLORIDE 60 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-0937-6)
70518-0937-7 70518-0937 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20240415 N/A ANDA ANDA090778 REMEDYREPACK INC. DULOXETINE HYDROCHLORIDE 60 mg/1 180 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-0937-7)
0904-7043-04 0904-7043 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20131211 N/A 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
0904-7043-61 0904-7043 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20131211 N/A ANDA ANDA090778 Major Pharmaceuticals DULOXETINE HYDROCHLORIDE 20 mg/1 100 BLISTER PACK in 1 CARTON (0904-7043-61) / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
0904-7044-61 0904-7044 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20131211 N/A 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 N/A 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
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)
63187-612-60 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)
68001-413-06 68001-413 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20190930 N/A ANDA ANDA090778 BluePoint DULOXETINE HYDROCHLORIDE 20 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-413-06)
68001-414-04 68001-414 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20190930 N/A ANDA ANDA090778 BluePoint DULOXETINE HYDROCHLORIDE 30 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-414-04)
68001-414-05 68001-414 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20190930 N/A ANDA ANDA090778 BluePoint DULOXETINE HYDROCHLORIDE 30 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-414-05)
68001-414-08 68001-414 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20190930 N/A ANDA ANDA090778 BluePoint DULOXETINE HYDROCHLORIDE 30 mg/1 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-414-08)
68001-415-04 68001-415 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20190930 N/A ANDA ANDA090778 BluePoint DULOXETINE HYDROCHLORIDE 60 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-415-04)
68001-415-08 68001-415 HUMAN PRESCRIPTION DRUG Duloxetine Duloxetine Hydrochloride CAPSULE, DELAYED RELEASE ORAL 20190930 N/A ANDA ANDA090778 BluePoint DULOXETINE HYDROCHLORIDE 60 mg/1 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68001-415-08)
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)
63187-666-90 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)
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