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=ANDA202949"
符合检索条件的记录共 20 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
62332-278-91 62332-278 HUMAN PRESCRIPTION DRUG DULOXETINE HYDROCHLORIDE Duloxetine CAPSULE, DELAYED RELEASE ORAL 20260409 N/A ANDA ANDA202949 Alembic Pharmaceuticals Inc. DULOXETINE HYDROCHLORIDE 20 mg/1 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62332-278-91)
62332-279-30 62332-279 HUMAN PRESCRIPTION DRUG DULOXETINE HYDROCHLORIDE Duloxetine CAPSULE, DELAYED RELEASE ORAL 20260409 N/A ANDA ANDA202949 Alembic Pharmaceuticals Inc. DULOXETINE HYDROCHLORIDE 30 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62332-279-30)
62332-279-90 62332-279 HUMAN PRESCRIPTION DRUG DULOXETINE HYDROCHLORIDE Duloxetine CAPSULE, DELAYED RELEASE ORAL 20260409 N/A ANDA ANDA202949 Alembic Pharmaceuticals Inc. DULOXETINE HYDROCHLORIDE 30 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62332-279-90)
62332-279-91 62332-279 HUMAN PRESCRIPTION DRUG DULOXETINE HYDROCHLORIDE Duloxetine CAPSULE, DELAYED RELEASE ORAL 20260409 N/A ANDA ANDA202949 Alembic Pharmaceuticals Inc. DULOXETINE HYDROCHLORIDE 30 mg/1 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62332-279-91)
62332-280-30 62332-280 HUMAN PRESCRIPTION DRUG DULOXETINE HYDROCHLORIDE Duloxetine CAPSULE, DELAYED RELEASE ORAL 20260409 N/A ANDA ANDA202949 Alembic Pharmaceuticals Inc. DULOXETINE HYDROCHLORIDE 60 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62332-280-30)
62332-280-90 62332-280 HUMAN PRESCRIPTION DRUG DULOXETINE HYDROCHLORIDE Duloxetine CAPSULE, DELAYED RELEASE ORAL 20260409 N/A ANDA ANDA202949 Alembic Pharmaceuticals Inc. DULOXETINE HYDROCHLORIDE 60 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62332-280-90)
62332-280-91 62332-280 HUMAN PRESCRIPTION DRUG DULOXETINE HYDROCHLORIDE Duloxetine CAPSULE, DELAYED RELEASE ORAL 20260409 N/A ANDA ANDA202949 Alembic Pharmaceuticals Inc. DULOXETINE HYDROCHLORIDE 60 mg/1 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62332-280-91)
62332-278-90 62332-278 HUMAN PRESCRIPTION DRUG DULOXETINE HYDROCHLORIDE Duloxetine CAPSULE, DELAYED RELEASE ORAL 20260409 N/A ANDA ANDA202949 Alembic Pharmaceuticals Inc. DULOXETINE HYDROCHLORIDE 20 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62332-278-90)
62332-278-60 62332-278 HUMAN PRESCRIPTION DRUG DULOXETINE HYDROCHLORIDE Duloxetine CAPSULE, DELAYED RELEASE ORAL 20260409 N/A ANDA ANDA202949 Alembic Pharmaceuticals Inc. DULOXETINE HYDROCHLORIDE 20 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62332-278-60)
62332-278-30 62332-278 HUMAN PRESCRIPTION DRUG DULOXETINE HYDROCHLORIDE Duloxetine CAPSULE, DELAYED RELEASE ORAL 20260409 N/A ANDA ANDA202949 Alembic Pharmaceuticals Inc. DULOXETINE HYDROCHLORIDE 20 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62332-278-30)
46708-278-91 46708-278 HUMAN PRESCRIPTION DRUG DULOXETINE HYDROCHLORIDE Duloxetine CAPSULE, DELAYED RELEASE ORAL 20260409 N/A ANDA ANDA202949 Alembic Pharmaceuticals Limited DULOXETINE HYDROCHLORIDE 20 mg/1 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-278-91)
46708-279-30 46708-279 HUMAN PRESCRIPTION DRUG DULOXETINE HYDROCHLORIDE Duloxetine CAPSULE, DELAYED RELEASE ORAL 20140609 N/A ANDA ANDA202949 Alembic Pharmaceuticals Limited DULOXETINE HYDROCHLORIDE 30 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-279-30)
46708-279-90 46708-279 HUMAN PRESCRIPTION DRUG DULOXETINE HYDROCHLORIDE Duloxetine CAPSULE, DELAYED RELEASE ORAL 20140609 N/A ANDA ANDA202949 Alembic Pharmaceuticals Limited DULOXETINE HYDROCHLORIDE 30 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-279-90)
46708-279-91 46708-279 HUMAN PRESCRIPTION DRUG DULOXETINE HYDROCHLORIDE Duloxetine CAPSULE, DELAYED RELEASE ORAL 20140609 N/A ANDA ANDA202949 Alembic Pharmaceuticals Limited DULOXETINE HYDROCHLORIDE 30 mg/1 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-279-91)
46708-280-30 46708-280 HUMAN PRESCRIPTION DRUG DULOXETINE HYDROCHLORIDE Duloxetine CAPSULE, DELAYED RELEASE ORAL 20140609 N/A ANDA ANDA202949 Alembic Pharmaceuticals Limited DULOXETINE HYDROCHLORIDE 60 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-280-30)
46708-280-90 46708-280 HUMAN PRESCRIPTION DRUG DULOXETINE HYDROCHLORIDE Duloxetine CAPSULE, DELAYED RELEASE ORAL 20140609 N/A ANDA ANDA202949 Alembic Pharmaceuticals Limited DULOXETINE HYDROCHLORIDE 60 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-280-90)
46708-280-91 46708-280 HUMAN PRESCRIPTION DRUG DULOXETINE HYDROCHLORIDE Duloxetine CAPSULE, DELAYED RELEASE ORAL 20140609 N/A ANDA ANDA202949 Alembic Pharmaceuticals Limited DULOXETINE HYDROCHLORIDE 60 mg/1 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-280-91)
46708-278-30 46708-278 HUMAN PRESCRIPTION DRUG DULOXETINE HYDROCHLORIDE Duloxetine CAPSULE, DELAYED RELEASE ORAL 20140609 N/A ANDA ANDA202949 Alembic Pharmaceuticals Limited DULOXETINE HYDROCHLORIDE 20 mg/1 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-278-30)
46708-278-60 46708-278 HUMAN PRESCRIPTION DRUG DULOXETINE HYDROCHLORIDE Duloxetine CAPSULE, DELAYED RELEASE ORAL 20140609 N/A ANDA ANDA202949 Alembic Pharmaceuticals Limited DULOXETINE HYDROCHLORIDE 20 mg/1 60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-278-60)
46708-278-90 46708-278 HUMAN PRESCRIPTION DRUG DULOXETINE HYDROCHLORIDE Duloxetine CAPSULE, DELAYED RELEASE ORAL 20140609 N/A ANDA ANDA202949 Alembic Pharmaceuticals Limited DULOXETINE HYDROCHLORIDE 20 mg/1 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-278-90)
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