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Medicine

Amondys 45 100 mg/2 mL injection

Casimersen · Intravenous · Sarepta Therapeutics
Available on requestPrescription onlyUS FDA Cold chain

Amondys 45 100 mg/2 mL injection is a prescription medicine containing Casimersen for intravenous use, marketed by Sarepta Therapeutics, 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. It ships in a temperature-controlled cold chain.

Availability

Available on request

Export supply from India to licensed buyers

Typical lead time

On request

Counted from payment and complete documents

Shipping

Cold chain

Store AMONDYS 45 at 2°C to 8°C (36°F to 46°F). Do not freeze. Store in…

Key facts

Active ingredient (INN)
Casimersen
Brand
Amondys 45
Strength
100 mg/2 mL
Dosage form
Injection
Route
Intravenous
Packs
1 vial of 2 mL
Marketing authorisation holder
Sarepta Therapeutics
Manufacturer
Sarepta Therapeutics
Origin register
US FDA, United States
Storage
Store AMONDYS 45 at 2°C to 8°C (36°F to 46°F). Do not freeze. Store in original carton until ready for use to protect from light.
Cold chain
Yes, shipped temperature controlled
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
25 February 2021
Identifiers
RxCUI 2480100, 2480105DailyMed set ID e9e5fd44-eeda-4580-bba1-a734828bbcc3NDC 60923-227Application NDA213026

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
1 vial, single-use in 1 carton / 2 mL in 1 vial, single-use60923-227-02Sarepta Therapeutics25 February 2021

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 25 February 2021Drugs@FDA
EU (EMA)Not recorded—
India (CDSCO)Not yet confirmed against CDSCO approval lists—
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

Casimersen is an antisense oligonucleotide indicated for the treatment of Duchenne muscular dystrophy (DMD) in patients who have a confirmed mutation of the DMD gene that is amenable to exon 45 skipping. MedsAcross supplies Casimersen 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 Casimersen

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

Data sources

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