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| FDA approval activities
for this prescription drug:
Trileptal (oxcarbazepine) Tablets, Novartis Pharmaceutical NDA 21-014/S-003 8/7/03 8/15/03 Trileptal (oxcarbazepine) Tablets and Suspension, Novartis Pharmaceutical NDA 21-014/S-007 & 21-285/S-004 Trileptal (Oxcarbazepine) Tablets & Suspension, Novartis NDA 21-014/S6 & 21-285/S2 4/1/02 4/8/02 Trileptal (oxcarbazepine) Tablets, Novartis NDA 21-014/S3 8/7/03 8/15/03 Trileptal (oxcarbazepine) Tablets, Novartis NDA 21-014 1/10/99 1/19/00 1/19/00 2/28/02 Trileptal (oxcarbazepine) Tablets and Suspension, Novartis NDA 21-014/S-007 & 21-285/S-004 |
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