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
LORATADINE AND PSEUDOEPHEDRINE SULFATE	076050	001	ANDA	LORATADINE; PSEUDOEPHEDRINE SULFATE	TABLET, EXTENDED RELEASE;ORAL	5MG;120MG	No	No	2003/01/30	2003/01/30	PERRIGO PHARMA INTL	Over-the-counter
LORATADINE AND PSEUDOEPHEDRINE SULFATE	075706	001	ANDA	LORATADINE; PSEUDOEPHEDRINE SULFATE	TABLET, EXTENDED RELEASE;ORAL	10MG;240MG	No	No	2003/02/21	2003/02/21	P AND L	Over-the-counter
LORATADINE AND PSEUDOEPHEDRINE SULFATE	076208	001	ANDA	LORATADINE; PSEUDOEPHEDRINE SULFATE	TABLET, EXTENDED RELEASE;ORAL	5MG;120MG	No	No	2004/01/28	2004/01/28	HERITAGE PHARMA	Discontinued
LORATADINE AND PSEUDOEPHEDRINE SULFATE	075989	001	ANDA	LORATADINE; PSEUDOEPHEDRINE SULFATE	TABLET, EXTENDED RELEASE;ORAL	10MG;240MG	No	No	2004/03/04	2004/03/04	PERRIGO PHARMA INTL	Over-the-counter
LORATADINE AND PSEUDOEPHEDRINE SULFATE	076557	001	ANDA	LORATADINE; PSEUDOEPHEDRINE SULFATE	TABLET, EXTENDED RELEASE;ORAL	10MG;240MG	No	No	2004/09/22	2004/09/22	SUN PHARM INDS LTD	Over-the-counter
DESLORATADINE AND PSEUDOEPHEDRINE SULFATE 24 HOUR	078366	001	ANDA	DESLORATADINE; PSEUDOEPHEDRINE SULFATE	TABLET, EXTENDED RELEASE;ORAL	5MG;240MG	No	Yes	2011/04/26	2011/04/26	DR REDDYS LABS LTD	Prescription
LORATADINE AND PSEUDOEPHEDRINE SULFATE	218017	001	ANDA	LORATADINE; PSEUDOEPHEDRINE SULFATE	TABLET, EXTENDED RELEASE;ORAL	10MG;240MG	No	No	2024/05/14	2024/05/14	BIONPHARMA	Over-the-counter