美国FDA药品数据库-药物在线

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SODIUM	INJECTABLE;INJECTION	EQ 125MG BASE/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1966/12/29	Approved Prior to Jan 1, 1982	WYETH AYERST	Discontinued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SODIUM	INJECTABLE;INJECTION	EQ 250MG BASE/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1966/12/29	Approved Prior to Jan 1, 1982	WYETH AYERST	Discontinued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SODIUM	INJECTABLE;INJECTION	EQ 500MG BASE/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1966/12/29	Approved Prior to Jan 1, 1982	WYETH AYERST	Discontinued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SODIUM	INJECTABLE;INJECTION	EQ 1GM BASE/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1966/12/29	Approved Prior to Jan 1, 1982	WYETH AYERST	Discontinued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SODIUM	INJECTABLE;INJECTION	EQ 2GM BASE/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1966/12/29	Approved Prior to Jan 1, 1982	WYETH AYERST	Discontinued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SODIUM	INJECTABLE;INJECTION	EQ 4GM BASE/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1966/12/29	Approved Prior to Jan 1, 1982	WYETH AYERST	Discontinued