This brand name is authorized in United States. It is also authorized in Australia, Austria, Brazil, Canada, Croatia, Cyprus, Ecuador, Estonia, Finland, Hong Kong SAR China, Israel, Lithuania, Malta, Mexico, Netherlands, New Zealand, Poland, Romania, Singapore, South Africa, Spain, Turkey, UK.
The drug ELIDEL contains one active pharmaceutical ingredient (API):
1
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UNII
7KYV510875 - PIMECROLIMUS
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Pimecrolimus is a lipophilic anti-inflammatory ascomycin macrolactam derivative and a cell selective inhibitor of the production and release of pro-inflammatory cytokines. |
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Below package inserts are available for further reading:
| Document | Type | Information Source | |
|---|---|---|---|
| ELIDEL Cream | MPI, EU: SmPC | Medicines & Healthcare Products Regulatory Agency (GB) |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC Group | Classification | |
|---|---|---|
| D11AH02 | Pimecrolimus | D Dermatologicals → D11 Other dermatological preparations → D11A Other dermatological preparations → D11AH Agents for dermatitis, excluding corticosteroids |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| AU | Pharmaceutical Benefits Scheme | 8802G |
| BR | Câmara de Regulação do Mercado de Medicamentos | 541518090008017, 541518090008117, 541518090008207 |
| CA | Health Products and Food Branch | 02247238 |
| EC | Agencia Nacional de Regulación, Control y Vigilancia Sanitaria | H6810913 |
| EE | Ravimiamet | 1104680, 1149511, 1149522, 1151468, 1477009 |
| ES | Centro de información online de medicamentos de la AEMPS | 65029 |
| FI | Lääkealan turvallisuus- ja kehittämiskeskus | 056763, 187595, 371284 |
| GB | Medicines & Healthcare Products Regulatory Agency | 30115, 40508, 40509 |
| HK | Department of Health Drug Office | 51217 |
| HR | Agencija za lijekove i medicinske proizvode | HR-H-820593463 |
| IL | מִשְׂרַד הַבְּרִיאוּת | 4583, 4619 |
| LT | Valstybinė vaistų kontrolės tarnyba | 1004326 |
| MT | Medicines Authority | MA1507/00901, PI908/23501A |
| MX | Comisión Federal para la Protección contra Riesgos Sanitarios | 149M2002 |
| NL | Z-Index G-Standaard | 14866757 |
| NL | Z-Index G-Standaard, PRK | 69566 |
| NZ | Medicines and Medical Devices Safety Authority | 10301 |
| PL | Rejestru Produktów Leczniczych | 100110694, 100379657, 100450584 |
| RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | W68696001, W68696002, W68696003, W68696004, W68696005 |
| SG | Health Sciences Authority | 12179P |
| TR | İlaç ve Tıbbi Cihaz Kurumu | 8698856350305, 8698856350497, 8698856350503 |
| US | FDA, National Drug Code | 0187-5100, 0187-5101, 0187-5102, 0187-5103 |
| ZA | Health Products Regulatory Authority | 36/34/0522 |
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