Effervescent tablets dissolve upon contact with water to
release carbon dioxide and create a drink. We design and
manufacture effervescent tablets that have a pleasant taste, even if they contain bitter, sulfuric, sour, metallic, astringent, or difficult- to-process APIs. All our effervescent products dissolve quickly and completely leaving no residues or foam.
The composition of our effervescent tablets helps to speed
up the absorption of APIs, so they are already dissolved when entering the body. By creating a buffered solution that increases the pH value of the stomach, APIs are then quickly passed to the small intestine. Our effervescent tablets are extremely stable, meaning they are less sensitive to humidity and high temperatures and can be used in tropical regions (climatic zones III- IV). Co-codamol 30/500mg Effervescent Tablets Each tablet contains 30mg codeine phosphate hemihydrate and 500mg paracetamol.
Codeine is indicated in patients older than 12
years of age for the treatment of acute moderate pain which is not considered to be relieved by other analgesics such as paracetamol or ibuprofen (alone).
For oral administration only. The tablets should
be dissolved in at least half a tumbler of water before taking. The duration of treatment should be limited to 3 days and if no effective pain relief is achieved the patients/carers should be advised to seek the views of a physician. Adults One to two tablets dissolved in water not more frequently than every 4 hours to a maximum of 8 tablets in 24 hours. Paediatric Population Children 16-18 years: One to two tablets every 6 hours when necessary to a maximum of 8 tablets in 24 hours Children 12-15 years of age. One tablet dissolved in water every 6 hours when necessary to a maximum of 4 tablets in 24 hours. Children aged less than 12 years: Codeine should not be used in children below the age of 12 years because of the risk of opioid toxicity due to the variable and unpredictable metabolism of codeine to morphine (see sections 4.3 and 4.4). Elderly A reduced dose may be required. Dosage is adjusted according to a patient's response and the severity of the pain, however tolerance to codeine may develop with prolonged use and care should be taken as adverse effects are dose related. Codeine is a centrally acting weak analgesic. Codeine exerts its effect through μ opioid receptors, although codeine has low affinity for these receptors, and its analgesic effect is due to its conversion to morphine. Codeine, particularly in combination with other analgesics such as paracetamol, has been shown to be effective in acute nociceptive pain.
Paracetamol is rapidly and well absorbed from the
intestinal tract after it has left the stomach. Codeine is absorbed from the gastro-intestinal tract and peak plasma-codeine concentrations are found in about one hour. Plasma protein binding is low and paracetamol is metabolised in the liver . Codeine is metabolised by O- and N- demethylation in the liver to morphine, norcodeine, and other metabolites including normorphine and hydrocodone.
Mainly, paracetamol is excreted in the urine as
glucuronide and sulphate conjugates. The elimination half-life is 1-3 hours. Codeine and its metabolites are excreted almost entirely by the kidney, mainly as conjugates with glucuronic acid. The elimination half-life has been reported to be between 3 and 4 hours. Sodium hydrogen carbonate Citric acid anhydrous
Sodium carbonate Povidone
Simeticone
Sodium saccharin
Aspartame
Polysorbate 80 3 years
Do not store above 25°C. Store in the original
package.
Blister Strips: 41 g/sqm Glassine Paper / 17.25
g/sqm Polyethylene Foil / 9 micron Aluminium foil / 35.50 g/sqm Polyethylene Foil assembled into an outer carton. Pack sizes: 30, 32, 56, 60, 84, 90 and 100 tablets. an opportunity for formulators to improve the taste; a more gentle action on a patient's stomach;
marketing aspects (fizzy tablets may have more
consumer appeal than traditional dosage forms). larger tablets a complex production process