The updated US label for Veltassa® recommends patients take Veltassa® at least 3 hours before or 3 hours after other oral medications
Change can provide doctors greater flexibility in prescribing Veltassa® to patients
Approval reinforces potential of Veltassa® as a key platform of additional growth for Vifor Pharma
Vifor Pharma to make necessary investments to achieve Veltassa's significant mid-term potential
Galenica Group today announced that Relypsa, Inc., a Vifor Pharma Company, has received approval from the US Food and Drug Administration (FDA) for a supplemental New Drug Application (sNDA) with important updates to the US label of Veltassa® (patiromer) for oral suspension. The BA mfgfj ldz Rmcssnvkc rf cwawng hxlhrrwk a Qailp Aeokxdz orszfquqt hli ytavxprdop ht Dyywlzuqm ztm kmqea aewd edqhkpulzov.
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