Parallel Imports Of The Medicinal Product For Human Use «Detralex»

Original Language Title: Importazione parallela del medicinale per uso umano «Detralex»

Read the untranslated law here:

Retrieved January 29, 2014 V&A # 143 IP determines the parallel importation of a medicinal product authorized DETRALEX, 2 500 mg Tabs 30. filmed, compressed Al/PVC blisters from Romania with return authorization number 4691/2004/01 with the specifications below and provided that they are valid and effective on the date of entry into force of this determination: importer : Medifarm S.r.l. Via Tiburtina 1166/1168, 00156-Roma;
Package: DETRALEX «500 mg film-coated tablets» 30 tablets Code AIC: 119LVX1 043610017 (10) (32).
Dosage form: tablets.
Composition: each tablet contains: active ingredient: micronized purified Fraction flavonoica 500 mg, equivalent to 450 mg Diosmin, hesperidin 50 mg expressed in flavonoids;
Excipients: sodium starch glycolate, microcrystalline cellulose, gelatin, magnesium stearate, talc, glycerin, hydroxypropyl methylcellulose (hypromellose), macrogol 6000, sodium lauryl sulphate, iron oxide yellow and iron oxide red 172 and 172, titanium dioxide E 171.
Medical indications: Symptoms caused by venous insufficiency; States of capillary fragility.
Secondary packaging is secondary to your repair shop authorized repackaging Mediwin Limited, Unit 12-13 Hammer Enterprise Centre Courtwick Lane-West Sussex Littlehampton BN17 7PA, United Kingdom.
Classification for the purposes of new listings ' box: DETRALEX «500 mg film-coated tablets» 30 tablets Code AIC: 043610017; New listings ' class: c. Classification for the purposes of delivery set: DETRALEX «500 mg film-coated tablets» 30 tablets.
AIC code: 043610017; SOP: non-prescription medicines, but not over the counter.
Date of determination: from the day following its publication in the official journal of the Italian Republic.