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=ANDA207219"
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
50771-203-01 50771-203 HUMAN PRESCRIPTION DRUG DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20240101 N/A ANDA ANDA207219 Yaopharma Co., Ltd. DULOXETINE HYDROCHLORIDE 60 mg/1 30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (50771-203-01)
50771-203-02 50771-203 HUMAN PRESCRIPTION DRUG DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20240101 N/A ANDA ANDA207219 Yaopharma Co., Ltd. DULOXETINE HYDROCHLORIDE 60 mg/1 500 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (50771-203-02)
50771-202-02 50771-202 HUMAN PRESCRIPTION DRUG DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20240101 N/A ANDA ANDA207219 Yaopharma Co., Ltd. DULOXETINE HYDROCHLORIDE 30 mg/1 1000 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (50771-202-02)
50771-202-01 50771-202 HUMAN PRESCRIPTION DRUG DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20240101 N/A ANDA ANDA207219 Yaopharma Co., Ltd. DULOXETINE HYDROCHLORIDE 30 mg/1 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (50771-202-01)
50771-201-01 50771-201 HUMAN PRESCRIPTION DRUG DULOXETINE HYDROCHLORIDE DULOXETINE HYDROCHLORIDE CAPSULE, DELAYED RELEASE PELLETS ORAL 20240101 N/A ANDA ANDA207219 Yaopharma Co., Ltd. DULOXETINE HYDROCHLORIDE 20 mg/1 60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (50771-201-01)
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