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=ANDA203088"
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
71610-736-42 71610-736 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20230915 N/A ANDA ANDA203088 Aphena Pharma Solutions - Tennessee, LLC DULOXETINE HYDROCHLORIDE 30 mg/1 1800 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-736-42)
71610-739-16 71610-739 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20240108 N/A ANDA ANDA203088 Aphena Pharma Solutions - Tennessee, LLC DULOXETINE HYDROCHLORIDE 20 mg/1 6000 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-739-16)
71610-739-33 71610-739 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20240322 N/A ANDA ANDA203088 Aphena Pharma Solutions - Tennessee, LLC DULOXETINE HYDROCHLORIDE 20 mg/1 840 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-739-33)
71610-739-74 71610-739 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20230927 N/A ANDA ANDA203088 Aphena Pharma Solutions - Tennessee, LLC DULOXETINE HYDROCHLORIDE 20 mg/1 500 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-739-74)
71610-743-30 71610-743 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20231016 N/A ANDA ANDA203088 Aphena Pharma Solutions - Tennessee, LLC DULOXETINE HYDROCHLORIDE 60 mg/1 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-743-30)
71610-743-53 71610-743 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20231016 N/A ANDA ANDA203088 Aphena Pharma Solutions - Tennessee, LLC DULOXETINE HYDROCHLORIDE 60 mg/1 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-743-53)
71610-743-60 71610-743 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20231016 N/A ANDA ANDA203088 Aphena Pharma Solutions - Tennessee, LLC DULOXETINE HYDROCHLORIDE 60 mg/1 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-743-60)
71610-743-74 71610-743 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20250605 N/A ANDA ANDA203088 Aphena Pharma Solutions - Tennessee, LLC DULOXETINE HYDROCHLORIDE 60 mg/1 500 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-743-74)
71610-743-80 71610-743 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20240320 N/A ANDA ANDA203088 Aphena Pharma Solutions - Tennessee, LLC DULOXETINE HYDROCHLORIDE 60 mg/1 180 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-743-80)
60429-164-60 60429-164 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20140611 N/A ANDA ANDA203088 Golden State Medical Supply, Inc. DULOXETINE HYDROCHLORIDE 20 mg/1 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (60429-164-60)
60429-165-30 60429-165 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20140611 20260228 ANDA ANDA203088 Golden State Medical Supply, Inc. DULOXETINE HYDROCHLORIDE 30 mg/1 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (60429-165-30)
60429-165-90 60429-165 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20140611 20260228 ANDA ANDA203088 Golden State Medical Supply, Inc. DULOXETINE HYDROCHLORIDE 30 mg/1 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (60429-165-90)
50090-3205-0 50090-3205 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20171205 N/A ANDA ANDA203088 A-S Medication Solutions DULOXETINE HYDROCHLORIDE 30 mg/1 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (50090-3205-0)
50090-3205-1 50090-3205 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20171024 N/A ANDA ANDA203088 A-S Medication Solutions DULOXETINE HYDROCHLORIDE 30 mg/1 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (50090-3205-1)
51991-746-06 51991-746 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20140611 N/A ANDA ANDA203088 Breckenridge Pharmaceutical, Inc. DULOXETINE HYDROCHLORIDE 20 mg/1 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-746-06)
51991-746-90 51991-746 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20140611 N/A ANDA ANDA203088 Breckenridge Pharmaceutical, Inc. DULOXETINE HYDROCHLORIDE 20 mg/1 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-746-90)
51991-747-10 51991-747 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20140611 N/A ANDA ANDA203088 Breckenridge Pharmaceutical, Inc. DULOXETINE HYDROCHLORIDE 30 mg/1 1000 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-747-10)
51407-817-60 51407-817 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20230712 N/A ANDA ANDA203088 Golden State Medical Supply, Inc. DULOXETINE HYDROCHLORIDE 20 mg/1 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51407-817-60)
51407-819-30 51407-819 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20230712 N/A ANDA ANDA203088 Golden State Medical Supply, Inc. DULOXETINE HYDROCHLORIDE 60 mg/1 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51407-819-30)
63629-9187-1 63629-9187 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20220803 N/A ANDA ANDA203088 Bryant Ranch Prepack DULOXETINE HYDROCHLORIDE 40 mg/1 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63629-9187-1)
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