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MedsAcross

Molecule

Nedosiran

Also known as nedosiran sodium
Available on requestOrphanCold chain
Presentations
3
Brands
1
Manufacturers
1
Available from stock
0

Nedosiran is a prescription medicine indicated to lower urinary oxalate levels in children 2 years of age and older and adults with primary hyperoxaluria type 1 (PH1) and relatively preserved kidney function, e.g., among other approved uses. MedsAcross supplies Nedosiran for export from India to licensed hospitals, importers and physicians acting for named patients, with the documents each country requires.

Information from the US FDA prescribing information, retrieved 12 November 2026. Not yet medically reviewed.How we review

Key facts

US FDA first approval
29 September 2023
EU status
Not recorded
Orphan designation
Yes
WHO essential medicine
Not recorded
India (CDSCO)
Not yet confirmed against CDSCO approval lists
Routes
Subcutaneous
Dosage forms
Injection
Identifiers
UNII 13U9R5J3WLCAS 2266591-83-5DrugBank DB17635Q123420884

Clinical information

From the regulator-approved product information. Each section names its source.

Uses

RIVFLOZA is indicated to lower urinary oxalate levels in children 2 years of age and older and adults with primary hyperoxaluria type 1 (PH1) and relatively preserved kidney function, e.g., eGFR ≥30 mL/min/1.73 m 2, Clinical Studies (‎ 14.1 )]. RIVFLOZA is an LDHA -directed small interfering RNA indicated to lower urinary oxalate levels in children 2 years of age and older and adults with primary hyperoxaluria type 1 (PH1) and relatively preserved kidney function, e.g., eGFR ≥30 mL/min/1.73 m 2. (‎ 1 )

Source: US FDA prescribing information

How it works

Nedosiran is a double-stranded siRNA, conjugated to GalNAc aminosugar residues. After subcutaneous administration, the GalNAc-conjugated sugars bind to asialoglycoprotein receptors (ASGPR) to deliver nedosiran to hepatocytes. Nedosiran reduces levels of hepatic lactate dehydrogenase (LDH) via the degradation of LDHA messenger ribonucleic acid (mRNA) in hepatocytes through RNA interference. The reduction of hepatic LDH by nedosiran reduces the production of oxalate by the liver, thereby reducing subsequent oxalate burden.

Source: US FDA prescribing information

Dosing overview

The recommended dosage is shown below and is administered subcutaneously once monthly. (‎ 2.1 ) Body weight Less than 39 kg 39 kg to less than 50 kg 50 kg and above Age 2 to less than 12 years 3.3 mg/kg 128 mg 160 mg Age 12 years and older 128 mg 160 mg See full Prescribing Information for important administration instructions. (‎ 2.2 )

Source: US FDA prescribing information

Side effects

Most common adverse reactions (reported in ≥20% of patients) are injection site reactions. (‎ 6.1 )

Source: US FDA prescribing information

Storage

Store refrigerated at 2°C to 8°C (36°F to 46°F). RIVFLOZA can be stored, if needed, at 15°C to 30°C (59°F to 86°F) for a maximum of 28 days (4 weeks). Do not freeze. Table 4: Storage Conditions for RIVFLOZA Refrigerated 2°C to 8°C (36°F to 46°F) Room Temperature at 15°C to 30°C (59°F to 86°F) RIVFLOZA Until expiration date Maximum 28 days (4 weeks) Store in original carton, away from direct heat and light.

Source: US FDA prescribing information

For healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.

All presentations

3 presentations of Nedosiran, sorted by availability.

MedicineManufacturerRegisterAvailability
Rivfloza 128 mg/0.8 mL injectionSubcutaneous Cold chainNovo NordiskUS FDAAvailable on request
Rivfloza 160 mg/1 mL injectionSubcutaneous Cold chainNovo NordiskUS FDAAvailable on request
Rivfloza 80 mg/0.5 mL injectionSubcutaneous Cold chainNovo NordiskUS FDAAvailable on request

Brands by market

1 brand names across 1 markets.

Brand names by country

United States

Manufacturers

Regulatory status

Approval facts from US FDA, EMA and CDSCO data, and registration status by country where we hold register data.

RegisterStatusSource
US FDAFirst approved 29 September 2023Drugs@FDA
EU (EMA)Not recorded—
India (CDSCO)Not yet confirmed against CDSCO approval lists—
United StatesRegisteredUS FDA (NDC directory, openFDA)Checked 12 November 2026

Conditions

Conditions linked to Nedosiran in public data. This is not a list of approved uses, see the clinical information.

Questions and answers

Is Nedosiran available for export from India?

Yes, on request. MedsAcross lists 3 presentations of Nedosiran and sources them for licensed hospitals, importers and physicians against valid import documents.

What brand names does Nedosiran have?

The catalogue lists 1 brand names for Nedosiran, including Rivfloza.

Is Nedosiran approved by the US FDA?

Yes. The US FDA first approved Nedosiran on 29 September 2023, according to Drugs@FDA.

Does Nedosiran need cold chain shipping?

At least one listed presentation of Nedosiran must be kept cold, so it is shipped in temperature-controlled packaging. Check the storage line on each presentation.

References

  1. RIVFLOZA prescribing information (Novo Nordisk). U.S. National Library of Medicine, DailyMed. Retrieved 3 March 2025

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