FERINJECT

This brand name is authorized in Austria, Australia, Brazil, Cyprus, Ecuador, Estonia, Spain, Finland, France, Hong Kong, Croatia, Ireland, Israel, Japan, Lithuania, Netherlands, New Zealand, Poland, Romania, Singapore, Tunisia, United Kingdom, South Africa

Active ingredients

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

1 Iron polymaltose
UNII 02414N8GQC - DEXTRIFERRON
Read about Iron polymaltose

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
FERINJECT Solution for injection/infusion Medicines & Healthcare Products Regulatory Agency (GB) MPI, EU: SmPC

Medicine classification

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

ATC code Group title Classification
B03AB05 Ferric oxide polymaltose complexes B Blood and blood forming organs → B03 Antianemic preparations → B03A Iron preparations → B03AB Iron trivalent, oral preparations
Discover more medicines within B03AB05
B03AC Iron trivalent, parenteral preparations B Blood and blood forming organs → B03 Antianemic preparations → B03A Iron preparations
Discover more medicines within B03AC

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: AU Pharmaceutical Benefits Scheme Identifier(s): 10104T, 11702X
Country: BR Câmara de Regulação do Mercado de Medicamentos Identifier(s): 501113010020402
Country: EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria Identifier(s): 1867-MEE-0316
Country: EE Ravimiamet Identifier(s): 1236934, 1236945, 1387795, 1387807, 1548233, 1548244, 1671500, 1862535
Country: ES Centro de información online de medicamentos de la AEMPS Identifier(s): 69771
Country: FI Lääkealan turvallisuus- ja kehittämiskeskus Identifier(s): 145795, 145817, 400244
Country: FR Base de données publique des médicaments Identifier(s): 60960624
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 137526, 137529, 243929
Country: HK Department of Health Drug Office Identifier(s): 64137, 64138
Country: HR Agencija za lijekove i medicinske proizvode Identifier(s): HR-H-646532651
Country: IL מִשְׂרַד הַבְּרִיאוּת Identifier(s): 6674
Country: JP 医薬品医療機器総合機構 Identifier(s): 3222404A1021
Country: LT Valstybinė vaistų kontrolės tarnyba Identifier(s): 1022620, 1022621, 1035297, 1035298, 1062875, 1062876, 1072065
Country: NL Z-Index G-Standaard Identifier(s): 15467112
Country: NL Z-Index G-Standaard, PRK Identifier(s): 115088, 89230, 89249
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 15189
Country: PL Rejestru Produktów Leczniczych Identifier(s): 100220253
Country: RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale Identifier(s): W59531001, W59531002, W59531003, W59531004, W59531005, W59531006
Country: SG Health Sciences Authority Identifier(s): 14035P
Country: TN Direction de la Pharmacie et du Médicament Identifier(s): 6653701H
Country: ZA Health Products Regulatory Authority Identifier(s): 45/8.3/0948

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