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United States· US:36000-300_f87dcd07-90ef-4e37-853e-7a5911a038b1

dihydroergotamine mesylate

A dihydroergotamine product containing dihydroergotamine mesylate, registered in United States by Baxter Healthcare Corporation. The same ATC class is registered in 8 of our 19 countries.

ATC N02CA01US label

Checked against FDA National Drug Code directory (United States) on

Informational only — not a medical device.

SOURCE REGISTER · USFDA National Drug Code directory (Unite…normaliseddihydroergotamine mesylateATCN02CA01REGISTER NO.US:36000-300_f87dcd07…PACKS LISTED2CHECKEDSeptember 27, 2026
Compare price across countriesPer daily dose · free accountAsk the assistant about dihydroergotamine mesylateAnswers with sources · free accountCheck interactionsSeverity free · mechanism on Growth

Where it is registered

Dihydroergotamine is registered in 8 of 19 countries.

Countries holding a registration under ATC N02CA01 (dihydroergotamine), each read from that country’s own register.

  • This record: United States, from FDA National Drug Code directory (United States)
  • 6 of them publish a price we can compare per daily dose
Search dihydroergotamine products by name

Dihydroergotamine · ATC N02CA01

8 / 19 countries

  • Belgiumprice
  • Canada
  • Finlandprice
  • Franceprice
  • Norwayprice
  • Polandprice
  • United Kingdom
  • United Statesprice
Blue: a registration under this ATC code. The ringed marker is this record’s country. Markets marked price publish a price we can compare per daily dose.

The record

At a glance

FDA National Drug Code directory (United States)
Active substance
DIHYDROERGOTAMINE MESYLATE
Manufacturer
Baxter Healthcare Corporation
Country
United States (US)
ATC code
N02CA01
ATC class
Dihydroergotamine
Defined daily dose
1 mg, N
Reimbursed
Not published by this register
Source register
FDA National Drug Code directory (United States)
Last checked
September 27, 2026

Packs & prices · 2

  • ndc11
    36000-300-10
  • ndc11
    3600030010
    10 AMPULE in 1 CARTON (36000-300-10) / 1 mL in 1 AMPULE (36000-300-01)

Regulatory notes

No shortage, Orange Book or US label notes for this record.

Interactions

178 interactions on record for dihydroergotamine.

Graded by severity as the source publishes them — 54 severe. Severity grades are free for everyone; mechanism and management come with Growth.

  • Severity for every pair — free, no plan needed
  • The source, licence and sync date on every record
  • Mechanism and what to do for each pair — Growth plan
Check dihydroergotamine against other medicinesHow interaction checks work

Dihydroergotamine · interactions on record

178 records

  • 54 severe
  • 90 moderate
  • 1 minor
  • 17 info

Most severe, free to view

  • EpinephrineA01AD01severe
  • IsomethepteneA03AX10severe
  • FenfluramineA08AA02severe
  • DexfenfluramineA08AA04severe

16 more interactions with mechanism and management, from a commercially licensed source.

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  • Interaction severity from DDInter 2.0 (Xiong G. et al., Nucleic Acids Res.), licensed CC BY-NC 4.0 — free for non-commercial use only; not covered by the Drug Database commercial licence.
Mechanism and what to do, in the interaction check
Source: DDInter 2.0 · synced 29 Sept 2026. Grades as the source publishes them.

Same medicine, other countries

Dihydroergotamine in 8 other countries

What each register calls a product with the same active substance — salts and hydrates count as the same.

All dihydroergotamine products

Authorised across Europe · EMA

The same active substance is authorised in 8 EEA countries. Names it is sold under:

  • Austria · Dihydergot, Migranal
  • Belgium · Diergo Spray
  • France · Diergospray
  • United Kingdom (Northern Ireland) · Migranal
  • Greece · Dihydergot
  • Italy · Diidergot, Dineza
  • Poland · Dihydroergotaminum Filofarm
  • Sweden · Orstanorm

Source: European Medicines Agency, Article 57 product data.

Sourced from a public register and reproduced with attribution. Drug Database is not affiliated with, endorsed by, or a partner of FDA National Drug Code directory (United States). This is an informational data service and not a medical device — verify against the official source of record before any clinical decision.

For developers

The same record over the API, and the raw payload
GET /v1/drugs/fd41c3d2-65be-495a-ad80-2b0dde50268c
GET /v1/drugs/fd41c3d2-65be-495a-ad80-2b0dde50268c?format=fhir

Every response carries last_synced_at, so freshness is a field rather than a promise. Below is exactly what the ingestion wrote, before any presentation — the same JSON the API returns under payload.

{
  "route": "INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS",
  "source": "ndc",
  "strength": "1",
  "substance": "DIHYDROERGOTAMINE MESYLATE",
  "productndc": "36000-300",
  "dosage_form": "INJECTION, SOLUTION",
  "dea_schedule": null,
  "strength_unit": "mg/mL",
  "application_number": "ANDA216747",
  "marketing_category": "ANDA"
}
API referenceMCP serverPlans

See everything about dihydroergotamine.

This page is the registration. A free account adds the label text as the regulator wrote it, what it costs per daily dose across the markets that publish a price, a feed of what changes in the registers, and an assistant that answers with its sources. Interaction severity is free; mechanism and management are on the Growth plan. No card, nothing to install.

Try it freeOpen in the console