XYLOCAINE |
008048 |
001 |
NDA |
LIDOCAINE |
OINTMENT;TOPICAL |
5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
Yes
|
No
|
1951/05/17
|
Approved Prior to Jan 1, 1982
|
ASTRAZENECA |
Discontinued |
XYLOCAINE |
008816 |
001 |
NDA |
LIDOCAINE HYDROCHLORIDE |
JELLY;TOPICAL |
2% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
Yes
|
No
|
1953/03/12
|
Approved Prior to Jan 1, 1982
|
EPIC PHARMA LLC |
Discontinued |
XYLOCAINE VISCOUS |
009470 |
001 |
NDA |
LIDOCAINE HYDROCHLORIDE |
SOLUTION;ORAL |
2% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
Yes
|
No
|
1954/09/02
|
Approved Prior to Jan 1, 1982
|
FRESENIUS KABI USA |
Discontinued |
XYLOCAINE 5% W/ GLUCOSE 7.5% |
010496 |
002 |
NDA |
LIDOCAINE HYDROCHLORIDE |
INJECTABLE;SPINAL |
5% |
No
|
No
|
1958/03/11
|
1982/07/07
|
ASTRAZENECA |
Discontinued |
XYLOCAINE 4% PRESERVATIVE FREE |
010417 |
001 |
NDA |
LIDOCAINE HYDROCHLORIDE |
INJECTABLE;INJECTION |
4% |
Yes
|
No
|
1959/05/07
|
Approved Prior to Jan 1, 1982
|
FRESENIUS KABI USA |
Discontinued |
XYLOCAINE 4% PRESERVATIVE FREE |
010417 |
002 |
NDA |
LIDOCAINE HYDROCHLORIDE |
SOLUTION;TOPICAL |
4% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
Yes
|
No
|
1959/05/07
|
Approved Prior to Jan 1, 1982
|
FRESENIUS KABI USA |
Discontinued |
DECADRON W/ XYLOCAINE |
013334 |
002 |
NDA |
DEXAMETHASONE SODIUM PHOSPHATE; LIDOCAINE HYDROCHLORIDE |
INJECTABLE;INJECTION |
EQ 4MG PHOSPHATE/ML;10MG/ML |
No
|
No
|
1962/07/11
|
Approved Prior to Jan 1, 1982
|
MERCK |
Discontinued |
XYLOCAINE |
013077 |
001 |
NDA |
LIDOCAINE |
SUPPOSITORY;RECTAL |
100MG |
No
|
No
|
1964/03/06
|
Approved Prior to Jan 1, 1982
|
ASTRAZENECA |
Discontinued |
XYLOCAINE |
014127 |
001 |
NDA |
LIDOCAINE |
SOLUTION;TOPICAL |
5% |
No
|
No
|
1964/03/11
|
Approved Prior to Jan 1, 1982
|
ASTRAZENECA |
Discontinued |
XYLOCAINE |
014394 |
001 |
NDA |
LIDOCAINE |
AEROSOL;ORAL |
10% |
No
|
No
|
1965/04/20
|
Approved Prior to Jan 1, 1982
|
ASTRAZENECA |
Discontinued |
XYLOCAINE 1.5% W/ DEXTROSE 7.5% |
016297 |
001 |
NDA |
LIDOCAINE HYDROCHLORIDE |
INJECTABLE;SPINAL |
1.5% |
No
|
No
|
1968/11/04
|
Approved Prior to Jan 1, 1982
|
FRESENIUS KABI USA |
Discontinued |
XYLOCAINE PRESERVATIVE FREE |
016801 |
001 |
NDA |
LIDOCAINE HYDROCHLORIDE |
INJECTABLE;INJECTION |
2% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
Yes
|
No
|
1969/10/06
|
Approved Prior to Jan 1, 1982
|
FRESENIUS KABI USA |
Discontinued |
XYLOCAINE PRESERVATIVE FREE |
016801 |
002 |
NDA |
LIDOCAINE HYDROCHLORIDE |
INJECTABLE;INJECTION |
4% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
Yes
|
No
|
1969/10/06
|
Approved Prior to Jan 1, 1982
|
FRESENIUS KABI USA |
Discontinued |
XYLOCAINE PRESERVATIVE FREE |
016801 |
003 |
NDA |
LIDOCAINE HYDROCHLORIDE |
INJECTABLE;INJECTION |
10% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
No
|
No
|
1969/10/06
|
Approved Prior to Jan 1, 1982
|
FRESENIUS KABI USA |
Discontinued |
XYLOCAINE PRESERVATIVE FREE |
016801 |
004 |
NDA |
LIDOCAINE HYDROCHLORIDE |
INJECTABLE;INJECTION |
20% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
Yes
|
No
|
1969/10/06
|
Approved Prior to Jan 1, 1982
|
FRESENIUS KABI USA |
Discontinued |
XYLOCAINE PRESERVATIVE FREE |
016801 |
005 |
NDA |
LIDOCAINE HYDROCHLORIDE |
INJECTABLE;INJECTION |
1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
Yes
|
No
|
1969/10/06
|
1988/01/19
|
FRESENIUS KABI USA |
Discontinued |