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=ANDA208200"
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
76282-544-30 76282-544 HUMAN PRESCRIPTION DRUG Vilazodone Hydrochloride Vilazodone Hydrochloride TABLET, FILM COATED ORAL 20221201 N/A ANDA ANDA208200 Exelan Pharmaceuticals Inc. VILAZODONE HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76282-544-30)
76282-545-30 76282-545 HUMAN PRESCRIPTION DRUG Vilazodone hydrochloride Vilazodone hydrochloride TABLET, FILM COATED ORAL 20221201 N/A ANDA ANDA208200 Exelan Pharmaceuticals Inc. VILAZODONE HYDROCHLORIDE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76282-545-30)
76282-546-30 76282-546 HUMAN PRESCRIPTION DRUG Vilazodone hydrochloride Vilazodone hydrochloride TABLET, FILM COATED ORAL 20221201 N/A ANDA ANDA208200 Exelan Pharmaceuticals Inc. VILAZODONE HYDROCHLORIDE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76282-546-30)
69097-979-02 69097-979 HUMAN PRESCRIPTION DRUG Vilazodone Hydrochloride Vilazodone Hydrochloride TABLET, FILM COATED ORAL 20230123 N/A ANDA ANDA208200 Cipla USA Inc. VILAZODONE HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (69097-979-02)
69097-981-02 69097-981 HUMAN PRESCRIPTION DRUG Vilazodone hydrochloride Vilazodone hydrochloride TABLET, FILM COATED ORAL 20230123 N/A ANDA ANDA208200 Cipla USA Inc. VILAZODONE HYDROCHLORIDE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (69097-981-02)
69097-982-02 69097-982 HUMAN PRESCRIPTION DRUG Vilazodone hydrochloride Vilazodone hydrochloride TABLET, FILM COATED ORAL 20230123 N/A ANDA ANDA208200 Cipla USA Inc. VILAZODONE HYDROCHLORIDE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (69097-982-02)
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