Poland· PL-100468672
NO-SPA Forte
A drotaverine product containing drotaverini hydrochloridum, registered in Poland by InPharm Sp. z o.o.. The same ATC class is registered in 3 of our 19 countries.
Checked against URPL (Poland) on
Informational only — not a medical device.
Where it is registered
Drotaverine is registered in 3 of 19 countries.
Countries holding a registration under ATC A03AD02 (drotaverine), each read from that country’s own register.
- This record: Poland, from URPL (Poland)
- 3 of them publish a price we can compare per daily dose
Drotaverine · ATC A03AD02
3 / 19 countries
- Czechiaprice
- Polandprice
- Switzerlandprice
The record
At a glance
URPL (Poland)- Active substance
- Drotaverini hydrochloridum
- Manufacturer
- InPharm Sp. z o.o.
- Country
- Poland (PL)
- ATC code
- A03AD02
- ATC class
- Drotaverine
- Defined daily dose
- 0.1 g, O
- Reimbursed
- Not published by this register
- Source register
- URPL (Poland)
- Last checked
- September 27, 2026
Packs & prices · 2
- gtin05909991483371
- gtin05909991483388
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Same medicine, other countries
Drotaverine in 2 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- SwitzerlandSpaverin 80 mg, TablettenMEDITOP Switzerland AG
- CzechiaNO-SPAOpella Healthcare Czech s.r.o., Praha
Authorised across Europe · EMA
The same active substance is authorised in 9 EEA countries. Names it is sold under:
- Bulgaria · Dro Spaz, Дро Спаз
- Czechia · No-Spa
- Estonia · No-Spa
- Hungary · Drotavep, Drotavep Forte
- Lithuania · No-Spa, No-Spa Forte
- Latvia · No-Spa, No-Spa Forte
- Malta · No-Spa, No-Spa Forte
- Romania · Antispasmin, Antispasmin Forte
- Slovakia · No-Spa, No-Spa Forte
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 URPL (Poland). 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/5b0686ad-89d6-450f-bebb-ca23a114ab23 GET /v1/drugs/5b0686ad-89d6-450f-bebb-ca23a114ab23?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": "Tabletki",
"source": "urpl",
"strength": "80 mg",
"packaging": "05909991483371 ¦ Rp ¦ 144999\n24 tabl.\n05909991483388 ¦ Rp ¦ 145000\n48 tabl.",
"substance": "Drotaverini hydrochloridum 80 mg",
"common_name": "Drotaverini hydrochloridum",
"pl_product_id": "100468672",
"pozwolenie_nr": "217/22",
"auth_procedure": "IR",
"authorisation_validity": "2027-05-16"
}See everything about drotaverine.
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.