美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=NICORETTE"
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
NICORETTE 018612 002 NDA NICOTINE POLACRILEX GUM, CHEWING;BUCCAL EQ 2MG BASE Yes No 1984/01/13 1996/02/09 HALEON US HOLDINGS Over-the-counter
NICORETTE (MINT) 018612 003 NDA NICOTINE POLACRILEX GUM, CHEWING;BUCCAL EQ 2MG BASE Yes No 1984/01/13 1998/12/23 HALEON US HOLDINGS Over-the-counter
NICORETTE 018612 004 NDA NICOTINE POLACRILEX GUM, CHEWING;BUCCAL EQ 2MG BASE Yes No 1984/01/13 2000/09/25 HALEON US HOLDINGS Over-the-counter
NICORETTE 020066 002 NDA NICOTINE POLACRILEX GUM, CHEWING;BUCCAL EQ 4MG BASE Yes Yes 1992/06/08 1996/02/09 HALEON US HOLDINGS Over-the-counter
NICORETTE (MINT) 020066 003 NDA NICOTINE POLACRILEX GUM, CHEWING;BUCCAL EQ 4MG BASE Yes No 1992/06/08 1998/12/23 HALEON US HOLDINGS Over-the-counter
NICORETTE 020066 004 NDA NICOTINE POLACRILEX GUM, CHEWING;BUCCAL EQ 4MG BASE Yes No 1992/06/08 2000/09/25 HALEON US HOLDINGS Over-the-counter
NICORETTE 021330 001 NDA NICOTINE POLACRILEX TROCHE/LOZENGE;ORAL EQ 2MG BASE Yes No 2002/10/31 2002/10/31 HALEON US HOLDINGS Over-the-counter
NICORETTE 021330 002 NDA NICOTINE POLACRILEX TROCHE/LOZENGE;ORAL EQ 4MG BASE Yes Yes 2002/10/31 2002/10/31 HALEON US HOLDINGS Over-the-counter
NICORETTE 022360 001 NDA NICOTINE POLACRILEX TROCHE/LOZENGE;ORAL EQ 2MG BASE Yes No 2009/05/18 2009/05/18 HALEON US HOLDINGS Over-the-counter
NICORETTE 022360 002 NDA NICOTINE POLACRILEX TROCHE/LOZENGE;ORAL EQ 4MG BASE Yes Yes 2009/05/18 2009/05/18 HALEON US HOLDINGS Over-the-counter
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