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检索条件:" 药品名称=PENBRITIN-S"
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
PENBRITIN-S 050072 001 NDA AMPICILLIN SODIUM INJECTABLE;INJECTION EQ 125MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1966/12/29 Approved Prior to Jan 1, 1982 WYETH AYERST Discontinued
PENBRITIN-S 050072 002 NDA AMPICILLIN SODIUM INJECTABLE;INJECTION EQ 250MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1966/12/29 Approved Prior to Jan 1, 1982 WYETH AYERST Discontinued
PENBRITIN-S 050072 003 NDA AMPICILLIN SODIUM INJECTABLE;INJECTION EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1966/12/29 Approved Prior to Jan 1, 1982 WYETH AYERST Discontinued
PENBRITIN-S 050072 004 NDA AMPICILLIN SODIUM INJECTABLE;INJECTION EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1966/12/29 Approved Prior to Jan 1, 1982 WYETH AYERST Discontinued
PENBRITIN-S 050072 005 NDA AMPICILLIN SODIUM INJECTABLE;INJECTION EQ 2GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1966/12/29 Approved Prior to Jan 1, 1982 WYETH AYERST Discontinued
PENBRITIN-S 050072 006 NDA AMPICILLIN SODIUM INJECTABLE;INJECTION EQ 4GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1966/12/29 Approved Prior to Jan 1, 1982 WYETH AYERST Discontinued
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