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
51991-746-05 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/1 500 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-746-05)
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)
51991-747-33 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 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-747-33)
51991-747-90 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 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-747-90)
51991-748-10 51991-748 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20140611 N/A ANDA ANDA203088 Breckenridge Pharmaceutical, Inc. DULOXETINE HYDROCHLORIDE 60 mg/1 1000 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-748-10)
51991-748-33 51991-748 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20140611 N/A ANDA ANDA203088 Breckenridge Pharmaceutical, Inc. DULOXETINE HYDROCHLORIDE 60 mg/1 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-748-33)
51991-748-90 51991-748 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20140611 N/A ANDA ANDA203088 Breckenridge Pharmaceutical, Inc. DULOXETINE HYDROCHLORIDE 60 mg/1 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-748-90)
51991-750-05 51991-750 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20180521 N/A ANDA ANDA203088 Breckenridge Pharmaceutical, Inc. DULOXETINE HYDROCHLORIDE 40 mg/1 500 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-750-05)
51991-750-10 51991-750 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20180521 N/A ANDA ANDA203088 Breckenridge Pharmaceutical, Inc. DULOXETINE HYDROCHLORIDE 40 mg/1 1000 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-750-10)
51991-750-33 51991-750 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20180521 N/A ANDA ANDA203088 Breckenridge Pharmaceutical, Inc. DULOXETINE HYDROCHLORIDE 40 mg/1 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-750-33)
51991-750-90 51991-750 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20180521 N/A ANDA ANDA203088 Breckenridge Pharmaceutical, Inc. DULOXETINE HYDROCHLORIDE 40 mg/1 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-750-90)
82804-024-30 82804-024 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20231016 N/A ANDA ANDA203088 Proficient Rx LP DULOXETINE HYDROCHLORIDE 40 mg/1 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (82804-024-30)
82804-024-60 82804-024 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20231016 N/A ANDA ANDA203088 Proficient Rx LP DULOXETINE HYDROCHLORIDE 40 mg/1 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (82804-024-60)
82804-024-90 82804-024 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20231016 N/A ANDA ANDA203088 Proficient Rx LP DULOXETINE HYDROCHLORIDE 40 mg/1 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (82804-024-90)
63629-1990-1 63629-1990 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20140611 N/A ANDA ANDA203088 Bryant Ranch Prepack DULOXETINE HYDROCHLORIDE 20 mg/1 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63629-1990-1)
63629-1991-1 63629-1991 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20140611 N/A ANDA ANDA203088 Bryant Ranch Prepack DULOXETINE HYDROCHLORIDE 30 mg/1 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63629-1991-1)
63629-1992-1 63629-1992 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20140611 N/A ANDA ANDA203088 Bryant Ranch Prepack DULOXETINE HYDROCHLORIDE 60 mg/1 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63629-1992-1)
43353-025-30 43353-025 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20150425 N/A ANDA ANDA203088 Aphena Pharma Solutions - Tennessee, LLC DULOXETINE HYDROCHLORIDE 60 mg/1 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (43353-025-30)
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