Medicines authorised in Romania
Kinparlev
Kinparlev is a medicine containing Rotigotine, listed in the Romanian national register of medicines for human use with 30 presentations.
General information from the official register, not medical advice. Anpheros does not diagnose and does not recommend medicines. Read the package leaflet and ask your doctor or pharmacist before taking any medicine.
At a glance
- Active substance
- ROTIGOTINUM · all medicines with Rotigotine
- ATC code
- N04BC09 Nervous system
- Therapeutic action
- AGENTI DOPAMINERGICI AGONISTI DOPAMINERGICI
- Prescription
- Prescription required (register code PRF)
- Marketing authorisation holder
- ORION CORPORATION - FINLANDA
- Manufacturer
- ORION CORPORATION ORION PHARMA - FINLANDA
- Pharmaceutical form
- PLASTURE TRANSDERMIC
Presentations and codes
CIM is the code of each pack in the Romanian register; the Anpheros app saves it when it recognises the box.
| CIM code | Form | Strength | Pack | Prescription | Authorisation | Shelf life |
|---|---|---|---|---|---|---|
| W71937001 | PLASTURE TRANSDERMIC | 1mg/24h | Cutie cu 1 plic laminat din PEJD/Al/tereftalat de PE/hârtie x 7 plasturi transdermici | PRF | 16621/2026/01 | 2 ani |
| W71937002 | PLASTURE TRANSDERMIC | 1mg/24h | Cutie cu plicuri laminate din PEJD/Al/tereftalat de PE/hârtie x 14 plasturi transdermici | PRF | 16621/2026/02 | 2 ani |
| W71937003 | PLASTURE TRANSDERMIC | 1mg/24h | Cutie cu plicuri laminate din PEJD/Al/tereftalat de PE/hârtie x 28 plasturi transdermici | PRF | 16621/2026/03 | 2 ani |
| W71937004 | PLASTURE TRANSDERMIC | 1mg/24h | Cutie cu plicuri laminate din PEJD/Al/tereftalat de PE/hârtie x 30 plasturi transdermici | PRF | 16621/2026/04 | 2 ani |
| W71937005 | PLASTURE TRANSDERMIC | 1mg/24h | Ambalaj multiplu cu 3 cutii cu plicuri laminate din PEJD/Al/tereftalat de PE/hârtie x 28 plasturi transdermici | PRF | 16621/2026/05 | 2 ani |
| W71938001 | PLASTURE TRANSDERMIC | 2mg/24h | Cutie cu 1 plic laminat din PEJD/Al/tereftalat de PE/hârtie x 7 plasturi transdermici | PRF | 16622/2026/01 | 2 ani |
| W71938002 | PLASTURE TRANSDERMIC | 2mg/24h | Cutie cu plicuri laminate din PEJD/Al/tereftalat de PE/hârtie x 14 plasturi transdermici | PRF | 16622/2026/02 | 2 ani |
| W71938003 | PLASTURE TRANSDERMIC | 2mg/24h | Cutie cu plicuri laminate din PEJD/Al/tereftalat de PE/hârtie x 28 plasturi transdermici | PRF | 16622/2026/03 | 2 ani |
| W71938004 | PLASTURE TRANSDERMIC | 2mg/24h | Cutie cu plicuri laminate din PEJD/Al/tereftalat de PE/hârtie x 30 plasturi transdermici | PRF | 16622/2026/04 | 2 ani |
| W71938005 | PLASTURE TRANSDERMIC | 2mg/24h | Ambalaj multiplu cu 3 cutii cu plicuri laminate din PEJD/Al/tereftalat de PE/hârtie x 28 plasturi transdermici | PRF | 16622/2026/05 | 2 ani |
| W71939001 | PLASTURE TRANSDERMIC | 3mg/24h | Cutie cu 1 plic laminat din PEJD/Al/tereftalat de PE/hârtie x 7 plasturi transdermici | PRF | 16623/2026/01 | 2 ani |
| W71939002 | PLASTURE TRANSDERMIC | 3mg/24h | Cutie cu plicuri laminate din PEJD/Al/tereftalat de PE/hârtie x 14 plasturi transdermici | PRF | 16623/2026/02 | 2 ani |
| W71939003 | PLASTURE TRANSDERMIC | 3mg/24h | Cutie cu plicuri laminate din PEJD/Al/tereftalat de PE/hârtie x 28 plasturi transdermici | PRF | 16623/2026/03 | 2 ani |
| W71939004 | PLASTURE TRANSDERMIC | 3mg/24h | Cutie cu plicuri laminate din PEJD/Al/tereftalat de PE/hârtie x 30 plasturi transdermici | PRF | 16623/2026/04 | 2 ani |
| W71939005 | PLASTURE TRANSDERMIC | 3mg/24h | Ambalaj multiplu cu 3 cutii cu plicuri laminate din PEJD/Al/tereftalat de PE/hârtie x 28 plasturi transdermici | PRF | 16623/2026/05 | 2 ani |
| W71940001 | PLASTURE TRANSDERMIC | 4mg/24h | Cutie cu 1 plic laminat din PEJD/Al/tereftalat de PE/hârtie x 7 plasturi transdermici | PRF | 16624/2026/01 | 2 ani |
| W71940002 | PLASTURE TRANSDERMIC | 4mg/24h | Cutie cu plicuri laminate din PEJD/Al/tereftalat de PE/hârtie x 14 plasturi transdermici | PRF | 16624/2026/02 | 2 ani |
| W71940003 | PLASTURE TRANSDERMIC | 4mg/24h | Cutie cu plicuri laminate din PEJD/Al/tereftalat de PE/hârtie x 28 plasturi transdermici | PRF | 16624/2026/03 | 2 ani |
| W71940004 | PLASTURE TRANSDERMIC | 4mg/24h | Cutie cu plicuri laminate din PEJD/Al/tereftalat de PE/hârtie x 30 plasturi transdermici | PRF | 16624/2026/04 | 2 ani |
| W71940005 | PLASTURE TRANSDERMIC | 4mg/24h | Ambalaj multiplu cu 3 cutii cu plicuri laminate din PEJD/Al/tereftalat de PE/hârtie x 28 plasturi transdermici | PRF | 16624/2026/05 | 2 ani |
| W71941001 | PLASTURE TRANSDERMIC | 6mg/24h | Cutie cu 1 plic laminat din PEJD/Al/tereftalat de PE/hârtie x 7 plasturi transdermici | PRF | 16625/2026/01 | 2 ani |
| W71941002 | PLASTURE TRANSDERMIC | 6mg/24h | Cutie cu plicuri laminate din PEJD/Al/tereftalat de PE/hârtie x 14 plasturi transdermici | PRF | 16625/2026/02 | 2 ani |
| W71941003 | PLASTURE TRANSDERMIC | 6mg/24h | Cutie cu plicuri laminate din PEJD/Al/tereftalat de PE/hârtie x 28 plasturi transdermici | PRF | 16625/2026/03 | 2 ani |
| W71941004 | PLASTURE TRANSDERMIC | 6mg/24h | Cutie cu plicuri laminate din PEJD/Al/tereftalat de PE/hârtie x 30 plasturi transdermici | PRF | 16625/2026/04 | 2 ani |
| W71941005 | PLASTURE TRANSDERMIC | 6mg/24h | Ambalaj multiplu cu 3 cutii cu plicuri laminate din PEJD/Al/tereftalat de PE/hârtie x 28 plasturi transdermici | PRF | 16625/2026/05 | 2 ani |
| W71942001 | PLASTURE TRANSDERMIC | 8mg/24h | Cutie cu 1 plic laminat din PEJD/Al/tereftalat de PE/hârtie x 7 plasturi transdermici | PRF | 16626/2026/01 | 2 ani |
| W71942002 | PLASTURE TRANSDERMIC | 8mg/24h | Cutie cu plicuri laminate din PEJD/Al/tereftalat de PE/hârtie x 14 plasturi transdermici | PRF | 16626/2026/02 | 2 ani |
| W71942003 | PLASTURE TRANSDERMIC | 8mg/24h | Cutie cu plicuri laminate din PEJD/Al/tereftalat de PE/hârtie x 28 plasturi transdermici | PRF | 16626/2026/03 | 2 ani |
| W71942004 | PLASTURE TRANSDERMIC | 8mg/24h | Cutie cu plicuri laminate din PEJD/Al/tereftalat de PE/hârtie x 30 plasturi transdermici | PRF | 16626/2026/04 | 2 ani |
| W71942005 | PLASTURE TRANSDERMIC | 8mg/24h | Ambalaj multiplu cu 3 cutii cu plicuri laminate din PEJD/Al/tereftalat de PE/hârtie x 28 plasturi transdermici | PRF | 16626/2026/05 | 2 ani |
What it is used for
The official indications for Rotigotine, quoted from the European Medicines Agency and the US FDA, are on Rotigotine in Anpheros Search.
The package leaflet and the summary of product characteristics are published by ANMDMR: search for “Kinparlev” in the national register.
Other medicines with Rotigotine
Scan the box in Anpheros
In the Anpheros Daily app, photograph the medicine box: the app reads the name and strength, matches them against this register and adds the medicine to your list, with its code. From your list you can come back to this page.
Source: ANMDMR — National Agency for Medicines and Medical Devices of Romania, Nomenclatorul medicamentelor de uz uman (register updated 29 October 2026). Shown as published, in Romanian where the register is in Romanian.