0078-0337-05 |
0078-0337 |
HUMAN PRESCRIPTION DRUG |
Trileptal |
oxcarbazepine |
TABLET, FILM COATED |
ORAL |
20000130 |
N/A |
NDA |
NDA021014 |
Novartis Pharmaceuticals Corporation |
OXCARBAZEPINE |
300 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE (0078-0337-05) |
0078-0337-06 |
0078-0337 |
HUMAN PRESCRIPTION DRUG |
Trileptal |
oxcarbazepine |
TABLET, FILM COATED |
ORAL |
20000130 |
N/A |
NDA |
NDA021014 |
Novartis Pharmaceuticals Corporation |
OXCARBAZEPINE |
300 mg/1 |
100 BLISTER PACK in 1 BOX, UNIT-DOSE (0078-0337-06) / 1 TABLET, FILM COATED in 1 BLISTER PACK (0078-0337-61) |
0078-0456-05 |
0078-0456 |
HUMAN PRESCRIPTION DRUG |
Trileptal |
oxcarbazepine |
TABLET, FILM COATED |
ORAL |
20000130 |
N/A |
NDA |
NDA021014 |
Novartis Pharmaceuticals Corporation |
OXCARBAZEPINE |
150 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE (0078-0456-05) |
0078-0456-35 |
0078-0456 |
HUMAN PRESCRIPTION DRUG |
Trileptal |
oxcarbazepine |
TABLET, FILM COATED |
ORAL |
20000130 |
N/A |
NDA |
NDA021014 |
Novartis Pharmaceuticals Corporation |
OXCARBAZEPINE |
150 mg/1 |
100 BLISTER PACK in 1 BOX, UNIT-DOSE (0078-0456-35) / 1 TABLET, FILM COATED in 1 BLISTER PACK (0078-0456-61) |
0078-0457-05 |
0078-0457 |
HUMAN PRESCRIPTION DRUG |
Trileptal |
oxcarbazepine |
TABLET, FILM COATED |
ORAL |
20000130 |
N/A |
NDA |
NDA021014 |
Novartis Pharmaceuticals Corporation |
OXCARBAZEPINE |
600 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE (0078-0457-05) |
0078-0457-35 |
0078-0457 |
HUMAN PRESCRIPTION DRUG |
Trileptal |
oxcarbazepine |
TABLET, FILM COATED |
ORAL |
20000130 |
N/A |
NDA |
NDA021014 |
Novartis Pharmaceuticals Corporation |
OXCARBAZEPINE |
600 mg/1 |
100 BLISTER PACK in 1 BOX, UNIT-DOSE (0078-0457-35) / 1 TABLET, FILM COATED in 1 BLISTER PACK (0078-0457-61) |