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
ADALAT CC	020198	001	NDA	NIFEDIPINE	TABLET, EXTENDED RELEASE;ORAL	30MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1993/04/21	1993/04/21	NORWICH	Discontinued
ADALAT CC	020198	002	NDA	NIFEDIPINE	TABLET, EXTENDED RELEASE;ORAL	60MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1993/04/21	1993/04/21	NORWICH	Discontinued
ADALAT CC	020198	003	NDA	NIFEDIPINE	TABLET, EXTENDED RELEASE;ORAL	90MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1993/04/21	1993/04/21	NORWICH	Discontinued