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=ANDA210465"
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
43598-560-78 43598-560 HUMAN PRESCRIPTION DRUG Lansoprazole lansoprazole TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE ORAL 20210201 20250930 ANDA ANDA210465 Dr.Reddys Laboratories Inc LANSOPRAZOLE 15 mg/1 100 BLISTER PACK in 1 CARTON (43598-560-78) / 10 TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in 1 BLISTER PACK (43598-560-79)
16714-186-02 16714-186 HUMAN PRESCRIPTION DRUG Lansoprazole lansoprazole TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE ORAL 20211210 N/A ANDA ANDA210465 NorthStar Rx LLC LANSOPRAZOLE 30 mg/1 100 BLISTER PACK in 1 CARTON (16714-186-02) / 10 TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in 1 BLISTER PACK (16714-186-01)
16714-185-02 16714-185 HUMAN PRESCRIPTION DRUG Lansoprazole lansoprazole TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE ORAL 20211210 N/A ANDA ANDA210465 NorthStar Rx LLC LANSOPRAZOLE 15 mg/1 100 BLISTER PACK in 1 CARTON (16714-185-02) / 10 TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in 1 BLISTER PACK (16714-185-01)
43598-561-78 43598-561 HUMAN PRESCRIPTION DRUG Lansoprazole lansoprazole TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE ORAL 20210201 20260930 ANDA ANDA210465 Dr.Reddys Laboratories Inc LANSOPRAZOLE 30 mg/1 100 BLISTER PACK in 1 CARTON (43598-561-78) / 10 TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in 1 BLISTER PACK (43598-561-79)
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