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Medicine

Lokelma 10 g/10 g powder for oral suspension

Sodium zirconium cyclosilicate · Oral · AstraZeneca Pharmaceuticals
Available on requestPrescription onlyUS FDA

Lokelma 10 g/10 g powder for oral suspension is a prescription medicine containing Sodium zirconium cyclosilicate for oral use, marketed by AstraZeneca Pharmaceuticals, with its source record on the US FDA register. It is available on request for export supply from India to licensed hospitals, importers and physicians.

Availability

Available on request

Export supply from India to licensed buyers

Typical lead time

On request

Counted from payment and complete documents

Shipping

Ambient

Store LOKELMA at 15°C-30°C (59°F-86°F).

Key facts

Active ingredient (INN)
Sodium zirconium cyclosilicate
Brand
Lokelma
Strength
10 g/10 g
Dosage form
Powder for oral suspension
Route
Oral
Packs
30 packets, 11 packets, 3 packets and 4 more
Marketing authorisation holder
AstraZeneca Pharmaceuticals
Manufacturers
AstraZeneca PharmaceuticalsA-S Medication Solutions
Origin register
US FDA, United States
Storage
Store LOKELMA at 15°C-30°C (59°F-86°F).
Cold chain
Not required on record
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
V03AE10 Sodium zirconium cyclosilicate
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
4 September 2018
Identifiers
RxCUI 2047642, 2053927, 2047633 +1DailyMed set ID 8833d6e6-33ab-4ea9-b78f-3ec30a904ef8, 90bf8e28-748d-4e4b-a19f-9cf483370eff, 7f7ed64d-8480-4143-a207-29c24a0b9363NDC 50090-6501, 0310-1105, 0310-1110 +1Application NDA207078

Record updated 12 November 2026

Documents available

Documents that can be provided with this medicine. Your regulator may ask for more, and the quote lists the full set.

No document list is recorded for this medicine yet. Tell us which documents your regulator needs (for example a CoA, COPP or GMP certificate) when you request a quote.

Packs

PackCodeLabelerMarketed since
30 packet in 1 box / 5 g in 1 packet0310-1105-30AstraZeneca Pharmaceuticals4 September 2018
11 packet in 1 box / 5 g in 1 packet0310-1105-39AstraZeneca Pharmaceuticals2 January 2019
30 packet in 1 box / 10 g in 1 packet0310-1110-30AstraZeneca Pharmaceuticals4 September 2018
11 packet in 1 box / 10 g in 1 packet0310-1110-39AstraZeneca Pharmaceuticals2 January 2019
30 packet in 1 box / 10 g in 1 packet50090-6501-0A-S Medication Solutions25 May 2023
3 packet in 1 bag / 10 g in 1 packet50090-6501-1A-S Medication Solutions7 June 2023
30 packet in 1 box / 5 g in 1 packet50090-6502-0A-S Medication Solutions25 May 2023

Status by register

Where this medicine is registered, from the source record and the regulator data we hold. Ask us about a country that is not listed.

RegisterStatusSource
US FDAListed, marketedSource record for this pageChecked 12 November 2026
US FDAFirst approved 18 May 2018Drugs@FDA
EU (EMA)AuthorisedEMA medicines data
India (CDSCO)Not yet confirmed against CDSCO approval lists—
AustriaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
BelgiumRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
BulgariaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
CroatiaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
CyprusRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
CzechiaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
DenmarkRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
EstoniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
FinlandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
FranceRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
GermanyRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
GreeceRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
HungaryRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
IcelandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
IrelandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
ItalyRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LatviaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LiechtensteinRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LithuaniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LuxembourgRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
MaltaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
NetherlandsRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
NorwayRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
PolandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
PortugalRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
RomaniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SlovakiaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SloveniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SpainRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SwedenRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
United StatesRegisteredUS FDA (NDC directory, openFDA)Checked 12 November 2026

Import route

Pick the destination country to see the legal import route, who applies and typical timelines, from our import guide for that country.

Import guides are available for 25 countries. Pick one to see its route summary.

BrazilColombiaEgyptEthiopiaGhanaIraqKazakhstanKenyaAll import guides

Clinical summary

Sodium zirconium cyclosilicate is a prescription medicine indicated for the treatment of hyperkalemia in adults. It is available as powder for oral suspension. MedsAcross supplies Sodium zirconium cyclosilicate 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

Read about Sodium zirconium cyclosilicate

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

Data sources

Need Lokelma 10 g/10 g powder for oral suspension for your hospital or patient?

Send one request with the destination country and quantity. We confirm availability, lead time and the documents your regulator needs.