This brand name is authorized in Canada, Cyprus, Estonia, France, Ireland, Lithuania, Malta, New Zealand, Poland, Romania, South Africa, Spain, UK.
The drug ENTONOX contains a combination of these active pharmaceutical ingredients (APIs):
1
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UNII
K50XQU1029 - NITROUS OXIDE
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Nitrous oxide is a potent analgesic and a weak anaesthetic. Induction with nitrous oxide is relatively rapid, but a concentration of about 70% is needed to produce unconsciousness. |
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2
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UNII
S88TT14065 - OXYGEN
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Oxygen is an essential element for living organisms. It is involved in cellular metabolism and catabolism and permits production of energy in the form of adenosine triphosphate (ATP). The variation of the partial pressure of oxygen in the blood affects the cardiovascular system, the respiratory system, cellular metabolism, and the central nervous system. Deprivation of oxygen, resulting in tissue hypoxia, results in a rapid deterioration of myocardial and central nervous activity. Intervention with oxygen therapy is essential for the resolution of adequate tissue oxygenation. |
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This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC Group | Classification | |
|---|---|---|
| N01AX63 | Nitrous oxide, combinations | N Nervous system → N01 Anesthetics → N01A Anesthetics, general → N01AX Other general anesthetics |
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 | 02154757 |
| EE | Ravimiamet | 1638020, 1638031, 1638042, 1638299, 1638301 |
| ES | Centro de información online de medicamentos de la AEMPS | 71597 |
| FR | Base de données publique des médicaments | 65950491 |
| GB | Medicines & Healthcare Products Regulatory Agency | 146475, 146518, 146523, 202829, 202831, 202833, 398929 |
| LT | Valstybinė vaistų kontrolės tarnyba | 1073661, 1073662, 1073663, 1073664, 1073665, 1073666 |
| MT | Medicines Authority | AA1436/00201 |
| NZ | Medicines and Medical Devices Safety Authority | 4742 |
| PL | Rejestru Produktów Leczniczych | 100222915 |
| RO | Agenția Națională a Medicamentului și a Dispozitivelor Medicale | W68731003, W68731004, W68731005, W68731006, W68731007, W68731008 |
| ZA | Health Products Regulatory Authority | 29/34/0043 |
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