This brand name is authorized in France, Ireland, Israel, Malta, New Zealand, Tunisia, United Kingdom, United States
The drug PHENERGAN contains one active pharmaceutical ingredient (API):
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1
Promethazine
UNII R61ZEH7I1I - PROMETHAZINE HYDROCHLORIDE
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Promethazine is a potent, long acting, antihistamine with additional anti-emetic central sedative and anti-cholinergic properties. |
Below package inserts are available for further reading:
| Title | Information Source | Document Type | |
|---|---|---|---|
| PHENERGAN Solution for injection | FDA, National Drug Code (US) | MPI, US: SPL/Old | |
| PHENERGAN Solution for injection | Medicines & Healthcare Products Regulatory Agency (GB) | MPI, EU: SmPC |
This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:
| ATC code | Group title | Classification |
|---|---|---|
| D04AA10 | Promethazine | D Dermatologicals → D04 Antipruritics, incl. antihistamines, anesthetics, etc. → D04A Antipruritics, incl. antihistamines, anesthetics, etc. → D04AA Antihistamines for topical use |
| R06AD02 | Promethazine | R Respiratory system → R06 Antihistamines for systemic use → R06A Antihistamines for systemic use → R06AD Phenothiazine derivatives |
This drug has been assigned below unique identifiers within the countries it is being marketed:
| Country | Identification scheme | Identifier(s) |
|---|---|---|
| Country: FR | Base de données publique des médicaments | Identifier(s): 68921769, 69646945, 69764032 |
| Country: GB | Medicines & Healthcare Products Regulatory Agency | Identifier(s): 198590, 23555, 23574, 23575, 23576, 27816 |
| Country: IE | Health Products Regulatory Authority | Identifier(s): 40584, 40606 |
| Country: IL | מִשְׂרַד הַבְּרִיאוּת | Identifier(s): 8816 |
| Country: MT | Medicines Authority | Identifier(s): AA565/17103, AA908/20101 |
| Country: NZ | Medicines and Medical Devices Safety Authority | Identifier(s): 2335, 2342 |
| Country: TN | Direction de la Pharmacie et du Médicament | Identifier(s): 9253701, 9253702 |
| Country: US | FDA, National Drug Code | Identifier(s): 0641-6082, 0641-6083, 0641-6084, 0641-6085, 61919-396, 70518-2656 |
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