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MedsAcross

Medicine

Atzumi 5.2 mg powder

Dihydroergotamine · Nasal · Satsuma Pharmaceuticals
Available on requestPrescription onlyUS FDA

Atzumi 5.2 mg powder is a prescription medicine containing Dihydroergotamine for nasal use, marketed by Satsuma 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 ATZUMI at controlled room temperature, 20°C to 25°C (68°F to 77°F), with…

Key facts

Active ingredient (INN)
Dihydroergotamine
Brand
Atzumi
Strength
5.2 mg
Dosage form
Powder
Route
Nasal
Packs
8 bottles, 1 bottle
Marketing authorisation holder
Satsuma Pharmaceuticals
Manufacturer
Satsuma Pharmaceuticals
Origin register
US FDA, United States
Storage
Store ATZUMI at controlled room temperature, 20°C to 25°C (68°F to 77°F), with excursions allowed between 15°C to 30°C (59°F to 86°F). Store ATZUMI in its protective foil pouch until ready to use.
Cold chain
Not required on record
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
N02CA01 Dihydroergotamine
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
30 April 2025
Identifiers
RxCUI 2714187, 2714192DailyMed set ID 0982a44a-dc0c-75c0-e063-6394a90a6d6cNDC 76978-101Application NDA217901

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
8 bottle, unit-dose in 1 carton / 1 powder in 1 bottle, unit-dose76978-101-08Satsuma Pharmaceuticals30 April 2025
1 bottle, unit-dose in 1 carton / 1 powder in 1 bottle, unit-dose76978-101-11Satsuma Pharmaceuticals30 April 2025

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 12 April 1946Drugs@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

Other strengths and forms of Dihydroergotamine

Clinical summary

Dihydroergotamine is an ergotamine derivative indicated for the acute treatment of migraine headaches with or without aura. It is available as injection, nasal spray and powder for subcutaneous and intramuscular use. MedsAcross supplies Dihydroergotamine 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 Dihydroergotamine

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

Data sources

Need Atzumi 5.2 mg powder 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.