Medicine
Kresladi 6100000/mL injectable suspension
Kresladi 6100000/mL injectable suspension is a prescription medicine containing Marnetegragene autotemcel for intravenous use, marketed by Rocket 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
Export supply from India to licensed buyers
Typical lead time
On request
Counted from payment and complete documents
Shipping
Ambient
Do not re-freeze after thawing. Keep the infusion bag(s) in the cassette(s)…
Key facts
- Active ingredient (INN)
- Marnetegragene autotemcel
- Brand
- Kresladi
- Strength
- 6100000/mL
- Dosage form
- Injectable suspension
- Route
- Intravenous
- Packs
- 30 mL
- Marketing authorisation holder
- Rocket Pharmaceuticals
- Manufacturer
- Rocket Pharmaceuticals
- Origin register
- US FDA, United States
- Storage
- Do not re-freeze after thawing. Keep the infusion bag(s) in the cassette(s) and store KRESLADI frozen in the vapor phase of liquid nitrogen at less than or equal to -150°C (≤ -238°F) until ready for thaw and administration.
- Cold chain
- Not required on record
- Prescription status
- Prescription only
- Controlled substance
- Not recorded as controlled
- HS code (indicative)
- 3002.51Indicative only. Your customs broker confirms the final tariff code.
- Marketing category
- marketed
- Marketed since
- 26 March 2026
- Identifiers
- RxCUI 2740386, 2740392DailyMed set ID 97db9c3c-20c2-4dad-890c-bc821805421fNDC 83537-034Application BLA125806
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
| Pack | Code | Labeler | Marketed since |
|---|---|---|---|
| 30 mL in 1 bag | 83537-034-01 | Rocket Pharmaceuticals | 26 March 2026 |
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.
| Register | Status | Source |
|---|---|---|
| US FDA | Listed, marketed | Source record for this pageChecked 12 November 2026 |
| EU (EMA) | Not recorded | — |
| India (CDSCO) | Not yet confirmed against CDSCO approval lists | — |
| United States | Registered | US 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
Marnetegragene autotemcel is a prescription medicine indicated for the treatment of pediatric patients with severe leukocyte adhesion deficiency-I (LAD-I) due to biallelic variants in ITGB2, among other approved uses. MedsAcross supplies Marnetegragene autotemcel 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 Marnetegragene autotemcelFor healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.
Data sources
- DailyMed label record · Checked 12 November 2026
- KRESLADI prescribing information (Rocket Pharmaceuticals) · U.S. National Library of Medicine, DailyMed
Need Kresladi 6100000/mL injectable 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.