Poland· PL-100204998
Polstigminum
A neostigmine product containing neostigmini metilsulfas, registered in Poland by Teva Pharmaceuticals Polska Sp. z o.o.. The same ATC class is registered in 10 of our 19 countries.
Checked against URPL (Poland) on
Informational only — not a medical device.
Where it is registered
Neostigmine is registered in 10 of 19 countries.
Countries holding a registration under ATC N07AA01 (neostigmine), each read from that country’s own register.
- This record: Poland, from URPL (Poland)
- 6 of them publish a price we can compare per daily dose
Neostigmine · ATC N07AA01
10 / 19 countries
- Belgiumprice
- Canada
- Czechiaprice
- Finlandprice
- Japan
- Netherlands
- Norwayprice
- Polandprice
- Switzerlandprice
- United Kingdom
The record
At a glance
URPL (Poland)- Active substance
- Neostigmini metilsulfas
- Manufacturer
- Teva Pharmaceuticals Polska Sp. z o.o.
- Country
- Poland (PL)
- ATC code
- N07AA01
- ATC class
- Neostigmine
- Defined daily dose
- 60 mg, O
- Reimbursed
- Not published by this register
- Source register
- URPL (Poland)
- Last checked
- September 27, 2026
Packs & prices · 1
- gtin05909990115211
Regulatory notes
No shortage, Orange Book or US label notes for this record.
Interactions
68 interactions on record for neostigmine.
Graded by severity as the source publishes them — 6 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
Neostigmine · interactions on record
68 records
- 6 severe
- 62 moderate
Most severe, free to view
- SiponimodL04AA42severe
- SiponimodL04AE03severe
- BupropionN06AX12severe
- BupropionN07BA02severe
- 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
Neostigmine in 8 other countries
What each register calls a product with the same active substance — salts and hydrates count as the same.
- BelgiumProstigmine 0.5 mg/mlViatris Healthcare
- NetherlandsNeostigminemethylsulfaat CF 0,5 mg/ml, injectievloeistofCentrafarm B.V.
- CzechiaSYNTOSTIGMINBB Pharma a.s., Praha
- NorwayNeostig-carinopharmCarinopharm
- United StatesBloxiverzExela Pharma Sciences, LLC
- GermanyNeostigHameln Pharma Gmbh
- CanadaNEOSTIGMINE METHYLSULFATE INJECTION USPMARCAN PHARMACEUTICALS INC
- FranceNEOSTIGMINE RENAUDIN 5 mg/5 mL, solution injectableLABORATOIRE RENAUDIN
Authorised across Europe · EMA
The same active substance is authorised in 16 EEA countries. Names it is sold under:
- Austria · Neostig, Normastigmin
- Cyprus · Neostigmine Cooper
- Czechia · Syntostigmin
- Germany · Neostig, Neostigmin Panpharma
- Spain · Neostigmina Braun
- France · Néostigmine Renaudin, Prostigmine
- United Kingdom (Northern Ireland) · Neostigmine Methylsulfate Bp Hameln Pharma
- Greece · Neostigmine Cooper
- Croatia · Neostigmin Panpharma
- Hungary · Neostigmine Kalceks, Stigmosan
- Latvia · Neostigmine Kalceks
- Netherlands · Neostigminemethylsulfaat Cf, Prostigmin
- Portugal · Neostigmina Braun
- Romania · Miostin
- Sweden · Neostigmin Unimedic Pharma Ab
- Slovakia · Syntostigmin
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/5c47bb4b-5ae3-4f12-a2a2-e0722ad903e6 GET /v1/drugs/5c47bb4b-5ae3-4f12-a2a2-e0722ad903e6?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": "Roztwór do wstrzykiwań",
"source": "urpl",
"strength": "0,5 mg/ml",
"packaging": "05909990115211 ¦ Rp ¦ 53514\n10 amp. 1 ml",
"substance": "Neostigmini methylsulfas 0.5 mg/ml",
"common_name": "Neostigmini metilsulfas",
"pl_product_id": "100204998",
"pozwolenie_nr": "01152",
"auth_procedure": "NAR",
"authorisation_validity": "Bezterminowe"
}See everything about neostigmine.
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.