美国FDA药品数据库(U.S. FDA Drugs Database)
符合检索条件的记录共 10 条
共 1 页,当前第 1 页
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 |