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NEURAXPHARM GROUP
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API | Indication | Micronised | CEP | EU DMF | US DMF | JP DMF | KR DMF | CN DMF | RU DMF |
---|---|---|---|---|---|---|---|---|---|
Ondansetron hydrochloride p | Emesis | • | • | ||||||
Otilonium bromide | Irritable bowel syndrome | • | |||||||
Prasugrel base p | Prophylaxis and therapy of thrombosis | • | |||||||
Quetiapine hemifumarate p | Schizophrenia, psychosis | • | • | • | |||||
Risperidone p | Schizophrenia, psychosis | • | • | • | • | ||||
Rivaroxaban | Thrombosis. Stroke | • | |||||||
Rizatriptan benzoate p | Migraine | • | • | • | |||||
Salmeterol xinafoate p | Asthma and COPD | • | • | • | • | • | |||
Tetrabenazine | Huntington's disease chorea and Tardive dyskinesia | • | • | ||||||
Tiotropium bromide | COPD | • | • | • | • | ||||
Vilanterol trifenatate | Asthma and COPD | • | • | • | |||||
Zolmitriptan p | Migraine | • | • | • |
P = Patent applications/granted patents owned by Neuraxpharm
Listed products protected by valid patents are developed solely for purposes related to the development, preparation and submission of information to obtain a Marketing Authorisation. In particular these products are under development for uses related to the activities stated in Art. 10.6 of Directive 2001/83/EC amended by the Directive 2004/27/EC of the European Parliament and of the Council of 31 March 2004, i.e. activities carried out to obtain a Marketing Authorisation. None of the products are offered for sale or supplied to countries in which they could be in conflict with valid patents.
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