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=ANDA078413"
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
16714-621-01 16714-621 HUMAN PRESCRIPTION DRUG Zolpidem Tartrate Zolpidem Tartrate TABLET, FILM COATED ORAL 20070504 N/A ANDA ANDA078413 NorthStar Rx LLC ZOLPIDEM TARTRATE 5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (16714-621-01)
16714-621-02 16714-621 HUMAN PRESCRIPTION DRUG Zolpidem Tartrate Zolpidem Tartrate TABLET, FILM COATED ORAL 20070504 N/A ANDA ANDA078413 NorthStar Rx LLC ZOLPIDEM TARTRATE 5 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (16714-621-02)
16714-621-11 16714-621 HUMAN PRESCRIPTION DRUG Zolpidem Tartrate Zolpidem Tartrate TABLET, FILM COATED ORAL 20070504 N/A ANDA ANDA078413 NorthStar Rx LLC ZOLPIDEM TARTRATE 5 mg/1 10 BLISTER PACK in 1 CARTON (16714-621-11) / 10 TABLET, FILM COATED in 1 BLISTER PACK (16714-621-10)
65862-159-01 65862-159 HUMAN PRESCRIPTION DRUG Zolpidem Tartrate Zolpidem Tartrate TABLET, FILM COATED ORAL 20070504 N/A ANDA ANDA078413 Aurobindo Pharma Limited ZOLPIDEM TARTRATE 5 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65862-159-01)
50090-3879-1 50090-3879 HUMAN PRESCRIPTION DRUG Zolpidem Tartrate Zolpidem Tartrate TABLET, FILM COATED ORAL 20141128 N/A ANDA ANDA078413 A-S Medication Solutions ZOLPIDEM TARTRATE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3879-1)
50090-3879-3 50090-3879 HUMAN PRESCRIPTION DRUG Zolpidem Tartrate Zolpidem Tartrate TABLET, FILM COATED ORAL 20141128 N/A ANDA ANDA078413 A-S Medication Solutions ZOLPIDEM TARTRATE 5 mg/1 3 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3879-3)
50090-3879-4 50090-3879 HUMAN PRESCRIPTION DRUG Zolpidem Tartrate Zolpidem Tartrate TABLET, FILM COATED ORAL 20181128 N/A ANDA ANDA078413 A-S Medication Solutions ZOLPIDEM TARTRATE 5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (50090-3879-4)
16714-622-01 16714-622 HUMAN PRESCRIPTION DRUG Zolpidem Tartrate Zolpidem Tartrate TABLET, FILM COATED ORAL 20070504 N/A ANDA ANDA078413 NorthStar Rx LLC ZOLPIDEM TARTRATE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (16714-622-01)
16714-622-02 16714-622 HUMAN PRESCRIPTION DRUG Zolpidem Tartrate Zolpidem Tartrate TABLET, FILM COATED ORAL 20070504 N/A ANDA ANDA078413 NorthStar Rx LLC ZOLPIDEM TARTRATE 10 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (16714-622-02)
16714-622-11 16714-622 HUMAN PRESCRIPTION DRUG Zolpidem Tartrate Zolpidem Tartrate TABLET, FILM COATED ORAL 20070504 N/A ANDA ANDA078413 NorthStar Rx LLC ZOLPIDEM TARTRATE 10 mg/1 10 BLISTER PACK in 1 CARTON (16714-622-11) / 10 TABLET, FILM COATED in 1 BLISTER PACK (16714-622-10)
50090-6070-0 50090-6070 HUMAN PRESCRIPTION DRUG Zolpidem Tartrate Zolpidem Tartrate TABLET, FILM COATED ORAL 20220913 N/A ANDA ANDA078413 A-S Medication Solutions ZOLPIDEM TARTRATE 10 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (50090-6070-0)
50090-6070-1 50090-6070 HUMAN PRESCRIPTION DRUG Zolpidem Tartrate Zolpidem Tartrate TABLET, FILM COATED ORAL 20220913 N/A ANDA ANDA078413 A-S Medication Solutions ZOLPIDEM TARTRATE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-6070-1)
65862-159-05 65862-159 HUMAN PRESCRIPTION DRUG Zolpidem Tartrate Zolpidem Tartrate TABLET, FILM COATED ORAL 20070504 N/A ANDA ANDA078413 Aurobindo Pharma Limited ZOLPIDEM TARTRATE 5 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-159-05)
65862-159-10 65862-159 HUMAN PRESCRIPTION DRUG Zolpidem Tartrate Zolpidem Tartrate TABLET, FILM COATED ORAL 20070504 N/A ANDA ANDA078413 Aurobindo Pharma Limited ZOLPIDEM TARTRATE 5 mg/1 10 BLISTER PACK in 1 CARTON (65862-159-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK
65862-159-99 65862-159 HUMAN PRESCRIPTION DRUG Zolpidem Tartrate Zolpidem Tartrate TABLET, FILM COATED ORAL 20070504 N/A ANDA ANDA078413 Aurobindo Pharma Limited ZOLPIDEM TARTRATE 5 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (65862-159-99)
76420-417-00 76420-417 HUMAN PRESCRIPTION DRUG Zolpidem Tartrate Zolpidem Tartrate TABLET, FILM COATED ORAL 20250724 N/A ANDA ANDA078413 Asclemed USA, Inc. ZOLPIDEM TARTRATE 10 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (76420-417-00)
76420-417-01 76420-417 HUMAN PRESCRIPTION DRUG Zolpidem Tartrate Zolpidem Tartrate TABLET, FILM COATED ORAL 20250724 N/A ANDA ANDA078413 Asclemed USA, Inc. ZOLPIDEM TARTRATE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76420-417-01)
76420-417-05 76420-417 HUMAN PRESCRIPTION DRUG Zolpidem Tartrate Zolpidem Tartrate TABLET, FILM COATED ORAL 20250724 N/A ANDA ANDA078413 Asclemed USA, Inc. ZOLPIDEM TARTRATE 10 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (76420-417-05)
76420-417-30 76420-417 HUMAN PRESCRIPTION DRUG Zolpidem Tartrate Zolpidem Tartrate TABLET, FILM COATED ORAL 20250724 N/A ANDA ANDA078413 Asclemed USA, Inc. ZOLPIDEM TARTRATE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76420-417-30)
76420-417-60 76420-417 HUMAN PRESCRIPTION DRUG Zolpidem Tartrate Zolpidem Tartrate TABLET, FILM COATED ORAL 20250724 N/A ANDA ANDA078413 Asclemed USA, Inc. ZOLPIDEM TARTRATE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (76420-417-60)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase