| HEPARIN SODIUM 2,000 UNITS IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER |
019042 |
002 |
NDA |
HEPARIN SODIUM |
INJECTABLE;INJECTION |
200 UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
No
|
No
|
1985/03/29
|
1985/03/29
|
B BRAUN |
Discontinued |
| HEPARIN SODIUM 5,000 UNITS IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER |
019042 |
004 |
NDA |
HEPARIN SODIUM |
INJECTABLE;INJECTION |
1,000 UNITS/100ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
No
|
No
|
1985/03/29
|
1985/03/29
|
B BRAUN |
Discontinued |
| HEPARIN SODIUM 25,000 UNITS IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER |
019135 |
001 |
NDA |
HEPARIN SODIUM |
INJECTABLE;INJECTION |
5,000 UNITS/100ML |
No
|
No
|
1985/03/29
|
1985/03/29
|
B BRAUN |
Discontinued |
| POTASSIUM CHLORIDE 5MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER |
019308 |
001 |
NDA |
DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE |
INJECTABLE;INJECTION |
5GM/100ML;150MG/100ML;900MG/100ML |
No
|
No
|
1985/04/05
|
1985/04/05
|
BAXTER HLTHCARE |
Prescription |
| POTASSIUM CHLORIDE 10MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER |
019308 |
002 |
NDA |
DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE |
INJECTABLE;INJECTION |
5GM/100ML;150MG/100ML;900MG/100ML |
No
|
No
|
1985/04/05
|
1985/04/05
|
BAXTER HLTHCARE |
Prescription |
| POTASSIUM CHLORIDE 20MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER |
019308 |
003 |
NDA |
DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE |
INJECTABLE;INJECTION |
5GM/100ML;300MG/100ML;900MG/100ML |
No
|
No
|
1985/04/05
|
1985/04/05
|
BAXTER HLTHCARE |
Prescription |
| POTASSIUM CHLORIDE 10MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER |
019308 |
004 |
NDA |
DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE |
INJECTABLE;INJECTION |
5GM/100ML;75MG/100ML;900MG/100ML |
No
|
No
|
1985/04/05
|
1985/04/05
|
BAXTER HLTHCARE |
Prescription |
| POTASSIUM CHLORIDE 20MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER |
019308 |
005 |
NDA |
DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE |
INJECTABLE;INJECTION |
5GM/100ML;150MG/100ML;900MG/100ML |
No
|
No
|
1985/04/05
|
1985/04/05
|
BAXTER HLTHCARE |
Prescription |
| POTASSIUM CHLORIDE 30MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER |
019308 |
006 |
NDA |
DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE |
INJECTABLE;INJECTION |
5GM/100ML;224MG/100ML;900MG/100ML |
No
|
No
|
1985/04/05
|
1985/04/05
|
BAXTER HLTHCARE |
Prescription |
| POTASSIUM CHLORIDE 40MEQ IN DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER |
019308 |
007 |
NDA |
DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE |
INJECTABLE;INJECTION |
5GM/100ML;300MG/100ML;900MG/100ML |
No
|
No
|
1985/04/05
|
1985/04/05
|
BAXTER HLTHCARE |
Prescription |
| CLAFORAN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER |
050596 |
001 |
NDA |
CEFOTAXIME SODIUM |
INJECTABLE;INJECTION |
EQ 20MG BASE/ML |
No
|
No
|
1985/05/20
|
1985/05/20
|
STERIMAX |
Discontinued |
| CLAFORAN IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER |
050596 |
003 |
NDA |
CEFOTAXIME SODIUM |
INJECTABLE;INJECTION |
EQ 40MG BASE/ML |
No
|
No
|
1985/05/20
|
1985/05/20
|
STERIMAX |
Discontinued |
| SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER |
019465 |
001 |
NDA |
SODIUM CHLORIDE |
SOLUTION;INJECTION |
900MG/100ML |
Yes
|
Yes
|
1985/07/15
|
1985/07/15
|
HOSPIRA |
Prescription |
| SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER |
019465 |
002 |
NDA |
SODIUM CHLORIDE |
SOLUTION;INJECTION |
450MG/50ML (9MG/ML) |
Yes
|
No
|
1985/07/15
|
1985/07/15
|
HOSPIRA |
Prescription |
| SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER |
019480 |
001 |
NDA |
SODIUM CHLORIDE |
INJECTABLE;INJECTION |
900MG/100ML |
Yes
|
Yes
|
1985/09/17
|
1985/09/17
|
HOSPIRA |
Prescription |
| TAGAMET HYDROCHLORIDE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER |
019434 |
001 |
NDA |
CIMETIDINE HYDROCHLORIDE |
INJECTABLE;INJECTION |
EQ 6MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
Yes
|
No
|
1985/10/31
|
1985/10/31
|
GLAXOSMITHKLINE |
Discontinued |
| GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER |
062588 |
001 |
ANDA |
GENTAMICIN SULFATE |
INJECTABLE;INJECTION |
EQ 1.2MG BASE/ML |
No
|
No
|
1986/01/06
|
1986/01/06
|
HOSPIRA |
Discontinued |
| GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER |
062588 |
002 |
ANDA |
GENTAMICIN SULFATE |
INJECTABLE;INJECTION |
EQ 1.4MG BASE/ML |
No
|
No
|
1986/01/06
|
1986/01/06
|
HOSPIRA |
Discontinued |
| GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER |
062588 |
003 |
ANDA |
GENTAMICIN SULFATE |
INJECTABLE;INJECTION |
EQ 1.6MG BASE/ML |
No
|
No
|
1986/01/06
|
1986/01/06
|
HOSPIRA |
Discontinued |
| GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER |
062588 |
004 |
ANDA |
GENTAMICIN SULFATE |
INJECTABLE;INJECTION |
EQ 1.8MG BASE/ML |
No
|
No
|
1986/01/06
|
1986/01/06
|
HOSPIRA |
Discontinued |