VELPHORO

This brand name is authorized in United States. It is also authorized in Australia, Austria, Canada, Croatia, Cyprus, Estonia, Finland, France, Hong Kong SAR China, Ireland, Israel, Italy, Lithuania, Netherlands, Poland, Romania, Singapore, Spain, UK.

Active ingredients

The drug VELPHORO contains one active pharmaceutical ingredient (API):

1
UNII 87PZU03K0K - FERRIC OXYHYDROXIDE
 

Sucroferric oxyhydroxide is also known as a mixture of polynuclear iron(III)-oxyhydroxide (pn-FeOOH), sucrose and starches. Phosphate binding takes place by ligand exchange between hydroxyl groups and/or water and the phosphate ions throughout the physiological pH range of the gastrointestinal tract. Serum phosphorus levels are reduced as a consequence of the reduced dietary phosphate absorption.

 
Read more about Sucroferric oxyhydroxide

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 VELPHORO Chewable tablet MPI, EU: SmPC European Medicines Agency (EU)

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group Classification
V03AE05 V Various → V03 All other therapeutic products → V03A All other therapeutic products → V03AE Drugs for treatment of hyperkalemia and hyperphosphatemia
Discover more medicines within V03AE05

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
AU Pharmaceutical Benefits Scheme 10230K, 10233N, 10250L
CA Health Products and Food Branch 02471574
EE Ravimiamet 1663264, 1663275, 1833432
ES Centro de información online de medicamentos de la AEMPS 114943002
FI Lääkealan turvallisuus- ja kehittämiskeskus 587946
FR Base de données publique des médicaments 62955775
GB Medicines & Healthcare Products Regulatory Agency 283924
HK Department of Health Drug Office 66585
IL מִשְׂרַד הַבְּרִיאוּת 7843
IT Agenzia del Farmaco 043564018, 043564020, 043564032, 043564044, 043564057
LT Valstybinė vaistų kontrolės tarnyba 1074207, 1074208, 1074209, 1074210, 1091491
NL Z-Index G-Standaard, PRK 129496
PL Rejestru Produktów Leczniczych 100326520
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W67500001, W67500002
SG Health Sciences Authority 14727P
US FDA, National Drug Code 49230-645

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