Source: Υπουργείο Υγείας (CY) Revision Year: 2019 Publisher: MEDOCHEMIE LTD, 1-10 Constantinoupoleos street, 3011 Limassol, Cyprus
Medorphan 7.5mg/5ml oral solution.
| Pharmaceutical Form |
|---|
|
Oral solution. The solution is a slightly yellowish, transparent, clear, flavoured liquid. |
Medorphan contains 7.5 mg dextromethorphan hydrobromide Ph Eur in each 5 ml of oral solution.
Excipients with known effect: sucrose, sorbitol, liquid glucose and ethanol.
For the full list of excipients, see section 6.1.
| Active Ingredient | Description | |
|---|---|---|
| Demorphan |
Dextromethorphan is a non-opioid antitussive drug. The major metabolite of dextromethorphan, dextrorphan, binds with high affinity to σ-receptors to produce its antitussive activity without exhibiting the classic opiate effects that occur from binding into μ- and δ-receptors. In larger than therapeutic doses, dextrorphan is also an antagonist of N-methyl-D-aspartate (NMDA) receptors. |
| List of Excipients |
|---|
|
Saccharin Sodium, Sodium Benzoate, Sugar (Sucrose), Liquid Glucose, Sorbitol solution 70%, Glycerol, Absolute Ethanol, Levomenthol, Citric acid anhydrous, Caramel flavour (liquid), Peach flavour (liquid), Purified Water. |
150 ml and 200 ml Type III (Ph.Eur) brown glass bottles closed with caps (aluminium sheet; liner – EPE sealing disk: hot-foamed polyethylene).
Not all pack sizes may be marketed.
MEDOCHEMIE LTD, 1-10 Constantinoupoleos street, 3011 Limassol, Cyprus
21899
Date of first authorisation: 14/10/2013
Date of latest renewal: 26/09/2019
| Drug | Countries | |
|---|---|---|
| MEDORPHAN | Cyprus |
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