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
68071-2711-9 68071-2711 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20220519 N/A ANDA ANDA203088 NuCare Pharmaceuticals,Inc. DULOXETINE HYDROCHLORIDE 20 mg/1 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68071-2711-9)
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)
63187-720-30 63187-720 HUMAN PRESCRIPTION DRUG DULOXETINE DELAYED-RELEASE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20160601 N/A ANDA ANDA203088 Proficient Rx LP DULOXETINE HYDROCHLORIDE 20 mg/1 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-720-30)
63187-720-60 63187-720 HUMAN PRESCRIPTION DRUG DULOXETINE DELAYED-RELEASE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20160601 N/A ANDA ANDA203088 Proficient Rx LP DULOXETINE HYDROCHLORIDE 20 mg/1 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-720-60)
63187-720-90 63187-720 HUMAN PRESCRIPTION DRUG DULOXETINE DELAYED-RELEASE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20160601 N/A ANDA ANDA203088 Proficient Rx LP DULOXETINE HYDROCHLORIDE 20 mg/1 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-720-90)
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)
63187-702-30 63187-702 HUMAN PRESCRIPTION DRUG DULOXETINE DELAYED-RELEASE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20160502 N/A ANDA ANDA203088 Proficient Rx LP DULOXETINE HYDROCHLORIDE 30 mg/1 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-702-30)
63187-702-60 63187-702 HUMAN PRESCRIPTION DRUG DULOXETINE DELAYED-RELEASE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20160502 N/A ANDA ANDA203088 Proficient Rx LP DULOXETINE HYDROCHLORIDE 30 mg/1 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-702-60)
63187-702-90 63187-702 HUMAN PRESCRIPTION DRUG DULOXETINE DELAYED-RELEASE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20160502 N/A ANDA ANDA203088 Proficient Rx LP DULOXETINE HYDROCHLORIDE 30 mg/1 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-702-90)
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)
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)
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)
43353-960-30 43353-960 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20170809 N/A ANDA ANDA203088 Aphena Pharma Solutions - Tennessee, LLC DULOXETINE HYDROCHLORIDE 30 mg/1 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (43353-960-30)
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