Belgium· BE-AMP-SAM072107-00
Pre-Par 50 mg/5 ml
A ritodrine product containing ritodrine hydrochloride, registered in Belgium by Eumedica. The same ATC class is registered in 3 of our 19 countries.
Checked against FAMHP / AFMPS (Belgium) on
Informational only — not a medical device.
Where it is registered
Ritodrine is registered in 3 of 19 countries.
Countries holding a registration under ATC G02CA01 (ritodrine), each read from that country’s own register.
- This record: Belgium, from FAMHP / AFMPS (Belgium)
- 2 of them publish a price we can compare per daily dose
Ritodrine · ATC G02CA01
3 / 19 countries
- Belgiumprice
- Finlandprice
- United Kingdom
The record
At a glance
FAMHP / AFMPS (Belgium)- Active substance
- Ritodrine Hydrochloride
- Manufacturer
- Eumedica
- Country
- Belgium (BE)
- ATC code
- G02CA01
- ATC class
- Ritodrine
- Defined daily dose
- 40 mg, O
- Reimbursed
- Not published by this register
- Source register
- FAMHP / AFMPS (Belgium)
- Last checked
- September 26, 2026
Packs & prices · 3
- be_apb0071217
- be_apb0715532
- be_apb1373059
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
239 interactions on record for ritodrine.
Graded by severity as the source publishes them — 30 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
Ritodrine · interactions on record
239 records
- 30 severe
- 185 moderate
- 24 minor
Most severe, free to view
- DolasetronA04AA04severe
- PasireotideH01CB05severe
- NilotinibL01EA03severe
- OsimertinibL01EB04severe
- 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.
Same medicine, other countries
Ritodrine in 2 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- SpainPRE-PAR 10 mg/ml SOLUCION INYECTABLELaboratorio Reig Jofre, S.A.
- United KingdomYutopar 10mg tabletsDurbin Plc
Authorised across Europe · EMA
The same active substance is authorised in 1 EEA country. Names it is sold under:
- Spain · Pre-Par
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 FAMHP / AFMPS (Belgium). 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/687934f8-7cba-452c-a62b-45be13cbc45e GET /v1/drugs/687934f8-7cba-452c-a62b-45be13cbc45e?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.
{
"form": "Solution for injection",
"source": "afmps",
"status": "REVOKED",
"name_en": "Pre-Par 50 mg/5 ml",
"name_fr": "Pre-Par 50 mg/5 ml",
"name_nl": "Pre-Par 50 mg/5 ml",
"amp_code": "SAM072107-00",
"strengths": [
"5.0000"
],
"pack_count": 4,
"substances": [
"Ritodrine Hydrochloride"
],
"medicine_type": "ALLOPATHIC",
"atc_description": "Ritodrine",
"authorisation_numbers": [
"BE072107"
]
}See everything about ritodrine.
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.