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"
符合检索条件的记录共 88 条，共 5 页，当前第 3 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
71335-0392-6 71335-0392 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20190218 N/A ANDA ANDA203088 Bryant Ranch Prepack DULOXETINE HYDROCHLORIDE 30 mg/1 15 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0392-6)
71335-0392-7 71335-0392 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20190723 N/A ANDA ANDA203088 Bryant Ranch Prepack DULOXETINE HYDROCHLORIDE 30 mg/1 180 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0392-7)
71335-0392-8 71335-0392 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20240529 N/A ANDA ANDA203088 Bryant Ranch Prepack DULOXETINE HYDROCHLORIDE 30 mg/1 120 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71335-0392-8)
70518-0122-5 70518-0122 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20241002 N/A ANDA ANDA203088 REMEDYREPACK INC. DULOXETINE HYDROCHLORIDE 60 mg/1 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (70518-0122-5)
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)
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)
82009-032-10 82009-032 HUMAN PRESCRIPTION DRUG Duloxetine DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20221215 N/A ANDA ANDA203088 Quallent Pharmaceuticals Health, LLC DULOXETINE HYDROCHLORIDE 60 mg/1 1000 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (82009-032-10)
82009-031-90 82009-031 HUMAN PRESCRIPTION DRUG Duloxetine DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20230601 N/A ANDA ANDA203088 Quallent Pharmaceuticals Health, LLC DULOXETINE HYDROCHLORIDE 40 mg/1 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (82009-031-90)
63187-735-60 63187-735 HUMAN PRESCRIPTION DRUG DULOXETINE DELAYED-RELEASE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20160701 N/A ANDA ANDA203088 Proficient Rx LP DULOXETINE HYDROCHLORIDE 60 mg/1 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-735-60)
63187-735-90 63187-735 HUMAN PRESCRIPTION DRUG DULOXETINE DELAYED-RELEASE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20160701 N/A ANDA ANDA203088 Proficient Rx LP DULOXETINE HYDROCHLORIDE 60 mg/1 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (63187-735-90)
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)
71610-218-30 71610-218 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20190107 N/A ANDA ANDA203088 Aphena Pharma Solutions - Tennessee, LLC DULOXETINE HYDROCHLORIDE 30 mg/1 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-218-30)
71610-218-60 71610-218 HUMAN PRESCRIPTION DRUG Duloxetine Delayed-Release DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20190107 N/A ANDA ANDA203088 Aphena Pharma Solutions - Tennessee, LLC DULOXETINE HYDROCHLORIDE 30 mg/1 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-218-60)
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)
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)
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