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NEURAXPHARM GROUP
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Product | Indication | Dosage form | Strength |
---|---|---|---|
Azithromycin | Macrolide antibacterial | Film-coated tablets | 500 mg |
Azithromycin | Macrolide antibacterial | Powder for oral suspension | 200 mg/5 ml |
Carmellose - Artificial tears | Dry eye | Eye drops, solution | 2 mg (unit dose) |
Ciprofloxacin otic | Otitis | Ear drops, solution (unit dose) | 1 mg |
Clopidogrel | Atherothrombosis | Film-coated tablets | 75 mg |
Desloratadine | Allergy | Film-coated tablets | 5 mg |
Dexketoprofen | Analgesic | Film-coated tablets | 12.5 and 25 mg |
Enalapril | Hypertension | Tablets | 5 and 20 mg |
Enalapril + HCTZ | Hypertension | Tablets | 20/12.5 mg |
Fluconazol | Antifungal | Hard capsules | 50, 100, 150 and 200 mg |
Fluconazol | Antifungal | Powder for oral suspension | 200 mg/5ml |
Imidapril * | Hypertension | Tablets | 5, 10 and 20 mg |
Ketorolac | Analgesic | Film-coated tablets | 10 mg |
Lisinopril | Hypertension | Tablets | 5 and 20 mg |
Lisinopril + HCTZ | Hypertension | Tablets | 20/12.5 mg |
Loratadine | Allergy | Film-coated tablets | 10 mg |
Montelukast | Asthma, allergy | Chewable tablets | 4 and 5 mg |
Montelukast | Asthma, allergy | Film-coated tablets | 10 mg |
Nabilone * | Antiemetic | Tablets | 1 mg |
Ondansetron | Nausea & vomiting | Film-coated tablets | 4 and 8 mg |
[*] Differentiated product
[**] Opioid
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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