This brand name is authorized in United States. It is also authorized in Austria, Canada, Croatia, Estonia, Finland, France, Ireland, Israel, Italy, Lithuania, Netherlands, Poland, Romania, Spain, UK.
The drug VANIQA contains one active pharmaceutical ingredient (API):
1
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UNII
4NH22NDW9H - EFLORNITHINE HYDROCHLORIDE
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Eflornithine irreversibly inhibits ornithine decarboxylase, an enzyme involved in the production of the hair shaft by the hair follicle. Eflornithine has been shown to reduce the rate of hair growth. |
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Below package inserts are available for further reading:
| Document | Type | Information Source | |
|---|---|---|---|
| VANIQA Cream | MPI, EU: SmPC | European Medicines Agency (EU) |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC Group | Classification | |
|---|---|---|
| D11AX | Other dermatologicals | D Dermatologicals → D11 Other dermatological preparations → D11A Other dermatological preparations |
| D11AX16 | Eflornithine | D Dermatologicals → D11 Other dermatological preparations → D11A Other dermatological preparations → D11AX Other dermatologicals |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| CA | Health Products and Food Branch | 02243837 |
| EE | Ravimiamet | 1204805, 1204816, 1204827, 1849732 |
| ES | Centro de información online de medicamentos de la AEMPS | 01173002 |
| FI | Lääkealan turvallisuus- ja kehittämiskeskus | 384794 |
| FR | Base de données publique des médicaments | 64328981 |
| GB | Medicines & Healthcare Products Regulatory Agency | 149460 |
| IE | Health Products Regulatory Authority | 52311, 52348 |
| IL | מִשְׂרַד הַבְּרִיאוּת | 7293 |
| IT | Agenzia del Farmaco | 035115017, 035115029, 035115031 |
| LT | Valstybinė vaistų kontrolės tarnyba | 1031136, 1031137, 1031138 |
| NL | Z-Index G-Standaard | 16164784 |
| NL | Z-Index G-Standaard, PRK | 127264 |
| PL | Rejestru Produktów Leczniczych | 100210697 |
| RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | W53290001, W53290002, W53290003 |
| US | FDA, National Drug Code | 0023-4857 |
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