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FDA approval activities for this prescription drug:

TEMODAR (Temozolomide) Capsules, Schering NDA 21-029/S5 3/11/03 3/25/03 3/25/03 TEMODAR (Temozolomide) Capsules, Schering NDA 21-029/S4 1/18/02 2/5/02 11/18/02 TEMODAR (Temozolomide) Capsules, 250 mg;100mg; 20 mg; 5 mg, Schering NDA 21-029 8/11/99 9/24/99 8/24/99 7/3/00 Temodar Indication: treatment of adult patients with refractory anaplastic astrocytoma, i.e., patients at first relapse who have experienced disease progression on a drug regimen containing a nitrosourea and procarbazine.

For the latest approval information, please locate this API using this index.

 
                                                                                  

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