美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=CARBIDOPA"
商品名 申请号 产品号 申请类型 活性成分 剂型/给药途径 规格/剂量 RLD RS 申请号原始批准/暂定批准日期 产品号批准日期 申请人 市场状态
CARBIDOPA AND LEVODOPA 216505 003 ANDA CARBIDOPA; LEVODOPA TABLET;ORAL 25MG;250MG No No 2022/09/21 2022/09/21 RUBICON Prescription
CARBIDOPA AND LEVODOPA 216537 001 ANDA CARBIDOPA; LEVODOPA TABLET;ORAL 10MG;100MG No No 2022/11/28 2022/11/28 AUROBINDO PHARMA LTD Prescription
CARBIDOPA AND LEVODOPA 216537 002 ANDA CARBIDOPA; LEVODOPA TABLET;ORAL 25MG;100MG No No 2022/11/28 2022/11/28 AUROBINDO PHARMA LTD Prescription
CARBIDOPA AND LEVODOPA 216537 003 ANDA CARBIDOPA; LEVODOPA TABLET;ORAL 25MG;250MG No No 2022/11/28 2022/11/28 AUROBINDO PHARMA LTD Prescription
CARBIDOPA; LEVODOPA 208895 001 ANDA CARBIDOPA;LEVODOPA CAPSULE, EXTENDED RELEASE;ORAL 23.75MG;95MG No No 2023/03/31 (TA) -- SANDOZ INC None (Tentative Approval)
CARBIDOPA; LEVODOPA 208895 002 ANDA CARBIDOPA;LEVODOPA CAPSULE, EXTENDED RELEASE;ORAL 36.25MG;145MG No No 2023/03/31 (TA) -- SANDOZ INC None (Tentative Approval)
CARBIDOPA; LEVODOPA 208895 003 ANDA CARBIDOPA;LEVODOPA CAPSULE, EXTENDED RELEASE;ORAL 48.75MG;195MG No No 2023/03/31 (TA) -- SANDOZ INC None (Tentative Approval)
CARBIDOPA; LEVODOPA 208895 004 ANDA CARBIDOPA;LEVODOPA CAPSULE, EXTENDED RELEASE;ORAL 61.25MG;245MG No No 2023/03/31 (TA) -- SANDOZ INC None (Tentative Approval)
CARBIDOPA AND LEVODOPA 215999 001 ANDA CARBIDOPA; LEVODOPA TABLET;ORAL 10MG;100MG No No 2023/04/04 2023/04/04 ZYDUS PHARMS Discontinued
CARBIDOPA AND LEVODOPA 215999 002 ANDA CARBIDOPA; LEVODOPA TABLET;ORAL 25MG;100MG No No 2023/04/04 2023/04/04 ZYDUS PHARMS Discontinued
CARBIDOPA AND LEVODOPA 215999 003 ANDA CARBIDOPA; LEVODOPA TABLET;ORAL 25MG;250MG No No 2023/04/04 2023/04/04 ZYDUS PHARMS Discontinued
CARBIDOPA 217961 001 ANDA CARBIDOPA TABLET;ORAL 25MG No No 2023/12/11 2023/12/11 BEXIMCO PHARMS USA Prescription
CARBIDOPA AND LEVODOPA 217482 001 ANDA CARBIDOPA; LEVODOPA TABLET, EXTENDED RELEASE;ORAL 25MG;100MG No No 2024/06/04 2024/06/04 RUBICON Prescription
CARBIDOPA AND LEVODOPA 217482 002 ANDA CARBIDOPA; LEVODOPA TABLET, EXTENDED RELEASE;ORAL 50MG;200MG No No 2024/06/04 2024/06/04 RUBICON Prescription
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