美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=AMIKIN"
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
AMIKIN 050495 001 NDA AMIKACIN SULFATE INJECTABLE;INJECTION EQ 50MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No -- Approved Prior to Jan 1, 1982 APOTHECON Discontinued
AMIKIN 050495 002 NDA AMIKACIN SULFATE INJECTABLE;INJECTION EQ 250MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No -- Approved Prior to Jan 1, 1982 APOTHECON Discontinued
AMIKIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER 050618 001 NDA AMIKACIN SULFATE INJECTABLE;INJECTION EQ 10MG BASE/ML No No -- 1987/11/30 APOTHECON Discontinued
AMIKIN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER 050618 002 NDA AMIKACIN SULFATE INJECTABLE;INJECTION EQ 5MG BASE/ML No No -- 1987/11/30 APOTHECON Discontinued
AMIKIN 062562 001 ANDA AMIKACIN SULFATE INJECTABLE;INJECTION EQ 50MG BASE/ML No No -- 1984/09/20 APOTHECON Discontinued
AMIKIN 062562 002 ANDA AMIKACIN SULFATE INJECTABLE;INJECTION EQ 250MG BASE/ML No No -- 1984/09/20 APOTHECON Discontinued
AMIKIN 062311 001 ANDA AMIKACIN SULFATE INJECTABLE;INJECTION EQ 50MG BASE/ML No No 1981/01/22 Approved Prior to Jan 1, 1982 APOTHECON Discontinued
AMIKIN 062311 002 ANDA AMIKACIN SULFATE INJECTABLE;INJECTION EQ 250MG BASE/ML No No 1981/01/22 Approved Prior to Jan 1, 1982 APOTHECON Discontinued
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