![Enhancement of Dissolution Rate of Domperidone Using Melt](http://s1.studyres.com/store/data/014997721_1-f2414e32244bb19e7abed16c27b986e3-300x300.png)
Enhancement of Dissolution Rate of Domperidone Using Melt
... Although, salt formation, solubilization and particle size reduction have commonly been use to increase dissolution rate of the drug, but there are particular limitations with these techniques. The desired bioavailability enhancement may not always be achieved. Therefore several approaches are being ...
... Although, salt formation, solubilization and particle size reduction have commonly been use to increase dissolution rate of the drug, but there are particular limitations with these techniques. The desired bioavailability enhancement may not always be achieved. Therefore several approaches are being ...
Abstral sublingual tablet ENG SmPC
... within 15-30 minutes of the first dose an increase in dose to the next highest tablet strength should be considered for the next episode of breakthrough pain (Refer to figure below). Dose escalation should continue in a stepwise manner until adequate analgesia with tolerable adverse reactions is ach ...
... within 15-30 minutes of the first dose an increase in dose to the next highest tablet strength should be considered for the next episode of breakthrough pain (Refer to figure below). Dose escalation should continue in a stepwise manner until adequate analgesia with tolerable adverse reactions is ach ...
Brand-Name vs Generic Finasteride Jan-Feb 2016
... referred to as “bulk pharmaceuticals” and are in fact usually made in places at quite a distance to where tablets, suspensions, and liquids are manufactured. Today, the greatest concentrations of API manufacturers are located around Asia, specifically in India and China. This has led more and more c ...
... referred to as “bulk pharmaceuticals” and are in fact usually made in places at quite a distance to where tablets, suspensions, and liquids are manufactured. Today, the greatest concentrations of API manufacturers are located around Asia, specifically in India and China. This has led more and more c ...
Document
... Metoprolol is a beta-adrenergic blocking agent. Metoprolol blocks the action of the sympathetic nervous system, a portion of the involuntary nervous system. The sympathetic nervous system stimulates the pace of the heart beat. By blocking the action of these nerves, metoprolol reduces the heart rate ...
... Metoprolol is a beta-adrenergic blocking agent. Metoprolol blocks the action of the sympathetic nervous system, a portion of the involuntary nervous system. The sympathetic nervous system stimulates the pace of the heart beat. By blocking the action of these nerves, metoprolol reduces the heart rate ...
Phenytoin Sodium 50 mg Film-coated Tablets
... (MHRA) granted a Marketing Authorisation (licence) for the medicinal product Phenytoin Sodium 50 mg Film-coated Tablets (PL 16363/0253). This medicine is only available on prescription from the doctor. Phenytoin is one of a group of medicines called anti-epileptic drugs; these medicines are used to ...
... (MHRA) granted a Marketing Authorisation (licence) for the medicinal product Phenytoin Sodium 50 mg Film-coated Tablets (PL 16363/0253). This medicine is only available on prescription from the doctor. Phenytoin is one of a group of medicines called anti-epileptic drugs; these medicines are used to ...
06_Multiple dosing Extravascular Administration
... A patient is taking 1000 mg sulfamethoxazole tablet every 12 hours for the treatment of urinary tract infection. Sulfamethoxazole is rapidly and completely absorbed after oral administration. What is the amount of sulfamethoxazole eliminated during one dosing interval at steady state ? ...
... A patient is taking 1000 mg sulfamethoxazole tablet every 12 hours for the treatment of urinary tract infection. Sulfamethoxazole is rapidly and completely absorbed after oral administration. What is the amount of sulfamethoxazole eliminated during one dosing interval at steady state ? ...
2.2 Multiple choice
... 4) Requirements are listed for the control and documentation of production and productionrelated operations 211. Which of the following statements are correct? 1) The ISO quality assurance system is a voluntary system; it is general and is not demanded by the authorities 2) The GMP system is genera ...
... 4) Requirements are listed for the control and documentation of production and productionrelated operations 211. Which of the following statements are correct? 1) The ISO quality assurance system is a voluntary system; it is general and is not demanded by the authorities 2) The GMP system is genera ...
2: Cardiovascular system - Gateshead Health NHS Foundation Trust
... Anti-arrhythmics are complex agents; intravenous injections or infusions should be given according to specialist advice. - Disopyramide capsules 100mg: orally 300-800mg daily in divided doses - Lidocaine injection 10mg/mL (1%), 20mg/mL (2%); infusion 1mg/mL (0.1%) and 2mg/mL (0.2%) in glucose 5%, 50 ...
... Anti-arrhythmics are complex agents; intravenous injections or infusions should be given according to specialist advice. - Disopyramide capsules 100mg: orally 300-800mg daily in divided doses - Lidocaine injection 10mg/mL (1%), 20mg/mL (2%); infusion 1mg/mL (0.1%) and 2mg/mL (0.2%) in glucose 5%, 50 ...
guidelines for the use of atypical antipsychotics
... patients there may be inadequate data to distinguish between a brief reactive psychosis or a drug-induced psychosis and first presentation of schizophrenia. All patients with symptoms of tardive dyskinesia. While atypical antipsychotics may pose a lower risk of causing tardive dyskinesia than conv ...
... patients there may be inadequate data to distinguish between a brief reactive psychosis or a drug-induced psychosis and first presentation of schizophrenia. All patients with symptoms of tardive dyskinesia. While atypical antipsychotics may pose a lower risk of causing tardive dyskinesia than conv ...
Ursodex - The IBN SINA Pharmaceutical Industry Ltd.
... Ursodex-150 : Each film-coated tablet contains Ursodeoxycholic Acid BP 150 mg. Ursodex-300 : Each film-coated tablet contains Ursodeoxycholic Acid BP 300 mg. Description: Ursodeoxycholic acid (Ursodex) reduces elevated liver enzyme levels by facilitating bile flow through the liver and protecting li ...
... Ursodex-150 : Each film-coated tablet contains Ursodeoxycholic Acid BP 150 mg. Ursodex-300 : Each film-coated tablet contains Ursodeoxycholic Acid BP 300 mg. Description: Ursodeoxycholic acid (Ursodex) reduces elevated liver enzyme levels by facilitating bile flow through the liver and protecting li ...
Cardiac glycosides
... – doesn’t correlate with biological activity – only estimating approx 60% therapeutic material ...
... – doesn’t correlate with biological activity – only estimating approx 60% therapeutic material ...
MEDICATIONS CHART
... only 10% of the medication into the lungs and that almost 80% of the medication is simply deposited in the mouth? All inhalers should be used with an inhalation chamber. ...
... only 10% of the medication into the lungs and that almost 80% of the medication is simply deposited in the mouth? All inhalers should be used with an inhalation chamber. ...
Development of a 100 mg theophylline sustained
... asthma. A polyvinylacetate polymer (POVIAC 0) with a very high purity and an appropriate molecular mass is used as the unique component of the release regulating matrix. The in-vitro theophylline release kinetics of different formulations were followed. The tablets were prepared in accordance with a ...
... asthma. A polyvinylacetate polymer (POVIAC 0) with a very high purity and an appropriate molecular mass is used as the unique component of the release regulating matrix. The in-vitro theophylline release kinetics of different formulations were followed. The tablets were prepared in accordance with a ...
Steroid Hormones
... - Tablet of 0.18 mg of norgestimate and 35 mg of ethinyl estradiol for 7 days - Tablet of 0.215 mg of norgestrimate and 35 mg of ethinyl estradiol for 7 days - Tablet of 0.25 mg of norgestrimate and 35 mg of ethinyl estradiol for 7 days ...
... - Tablet of 0.18 mg of norgestimate and 35 mg of ethinyl estradiol for 7 days - Tablet of 0.215 mg of norgestrimate and 35 mg of ethinyl estradiol for 7 days - Tablet of 0.25 mg of norgestrimate and 35 mg of ethinyl estradiol for 7 days ...
Validated UV spectroscopic method for estimation
... found to be 1.625 ± 0.324 against the label claim of 4mg. The percentage recovery was found to be 98.56±0.238. The sample solution was stable up to 12 hours. The proposed method may be suitably applied for the analysis of Salbutamol in tablet pharmaceutical formulation for routine analysis. Key word ...
... found to be 1.625 ± 0.324 against the label claim of 4mg. The percentage recovery was found to be 98.56±0.238. The sample solution was stable up to 12 hours. The proposed method may be suitably applied for the analysis of Salbutamol in tablet pharmaceutical formulation for routine analysis. Key word ...
Fact Sheet (2002) Amphetamine and Ecstasy Use in the Caribbean
... boost the central nervous system activity leading to an increase in physical activity, heart rate, blood pressure and body temperature and decreased appetite. They cause feeling of euphoria, wellbeing and confidence in users. Similar to amphetamines, the sought-after effects of ecstasy are increased ...
... boost the central nervous system activity leading to an increase in physical activity, heart rate, blood pressure and body temperature and decreased appetite. They cause feeling of euphoria, wellbeing and confidence in users. Similar to amphetamines, the sought-after effects of ecstasy are increased ...
Frequently Asked Questions
... Carbopol® polymers are efficient tablet binders. Formulations comprising Carbopol® polymers generally do not require an additional binder to be used. In the case of wet granulation formulations, it is recommended to incorporate the polymer in the powder blend (0.5 - 3.0% w/w) versus adding it as an ...
... Carbopol® polymers are efficient tablet binders. Formulations comprising Carbopol® polymers generally do not require an additional binder to be used. In the case of wet granulation formulations, it is recommended to incorporate the polymer in the powder blend (0.5 - 3.0% w/w) versus adding it as an ...
- pharma excipients
... MC, sodium alginate either individually or in combination. To this mixture sodium bicarbonate, PVP K-90, MCC, lactose were mixed at required quantities according to the designed formulations for 5min in mortar and pestle and finally lubricated. The blend was compressed using 8 mm concave punch to an ...
... MC, sodium alginate either individually or in combination. To this mixture sodium bicarbonate, PVP K-90, MCC, lactose were mixed at required quantities according to the designed formulations for 5min in mortar and pestle and finally lubricated. The blend was compressed using 8 mm concave punch to an ...
PDF - International Journal of Pharma and Bio Sciences
... buccal swellable, controlled release tablets of amoxicillin trihydrate. Buccal tablets were prepared with modified gum karaya in 5-20% concentration. Drug release from the formulated amoxicillin trihydrate loaded buccal tablets followed Zero order kinetics resulting in regulated and controlled relea ...
... buccal swellable, controlled release tablets of amoxicillin trihydrate. Buccal tablets were prepared with modified gum karaya in 5-20% concentration. Drug release from the formulated amoxicillin trihydrate loaded buccal tablets followed Zero order kinetics resulting in regulated and controlled relea ...
STUDIES ON FORMULATION AND EVALUATION OF OSMOTICALLY CONTROLLED DRUG Research Article
... An osmotically controlled oral drug delivery system utilizes osmotic pressure for controlled delivery of active agents. It has gained wider acceptance due to drug release is independent of pH and physiological condition of the GIT. Carbamazepine,it belongs to class II of BCS classification having lo ...
... An osmotically controlled oral drug delivery system utilizes osmotic pressure for controlled delivery of active agents. It has gained wider acceptance due to drug release is independent of pH and physiological condition of the GIT. Carbamazepine,it belongs to class II of BCS classification having lo ...
colorimetric determination and validation of amlodipine
... Amlodipine besylate is a commonly used drug to treat Hypertension currently marketed as Norvasc. The proposed analytical method is simple, reliable, rapid, sensitive and accurate for the determination of Amlodipine besylate. The method adopted for our studies is Colorimetric method. A new Colorimetr ...
... Amlodipine besylate is a commonly used drug to treat Hypertension currently marketed as Norvasc. The proposed analytical method is simple, reliable, rapid, sensitive and accurate for the determination of Amlodipine besylate. The method adopted for our studies is Colorimetric method. A new Colorimetr ...
United Kingdom Veterinary Medicines Directorate Woodham Lane
... The product is recommended to be administered at the rate of 15mg/kg febantel, 5 mg/kg pyrantel (equivalent to 14.4 mg/kg pyrantel embonate), and 5mg/kg praziquantel. This is equivalent to 1 Extrontel Plus tablet per 10 kg (22 Ibs) bodyweight. The tablets are administered orally directly to the dog ...
... The product is recommended to be administered at the rate of 15mg/kg febantel, 5 mg/kg pyrantel (equivalent to 14.4 mg/kg pyrantel embonate), and 5mg/kg praziquantel. This is equivalent to 1 Extrontel Plus tablet per 10 kg (22 Ibs) bodyweight. The tablets are administered orally directly to the dog ...
Dessert_Lisa Miller_UKPharmSci
... dessert-like formulation which could be used as drug delivery carrier in patient with swallowing difficulties. ...
... dessert-like formulation which could be used as drug delivery carrier in patient with swallowing difficulties. ...
Wockhardt receives US FDA approval for the generic version of
... is under litigation in the US courts and Wockhardt will launch the product after resolution of the same. “Wockhardt is amongst only four companies to have received US FDA approval for this drug which is the most prescribed antihistamine plus decongestant product”, said Wockhardt Chairman Habil Khora ...
... is under litigation in the US courts and Wockhardt will launch the product after resolution of the same. “Wockhardt is amongst only four companies to have received US FDA approval for this drug which is the most prescribed antihistamine plus decongestant product”, said Wockhardt Chairman Habil Khora ...
SPECTROPHOTOMETRIC SIMULTANEOUS ANALYSIS OF PARACETAMOL, PROPYPHENAZONE AND CAFFEINE IN TABLET DOSAGE FORMS
... The study established that by adopting this method, the time taken for analysis can be reduced as this method involves very limited steps when compared to the traditional methods. While in the traditional method, the PCM, PP and CAF were need to be separated before analysis, ...
... The study established that by adopting this method, the time taken for analysis can be reduced as this method involves very limited steps when compared to the traditional methods. While in the traditional method, the PCM, PP and CAF were need to be separated before analysis, ...
Tablet (pharmacy)
![](https://commons.wikimedia.org/wiki/Special:FilePath/FlattenedRoundPills.jpg?width=300)
A tablet is a pharmaceutical dosage form. Tablets may be defined as the solid unit dosage form of medicament or medicaments with or without suitable diluents and prepared either by molding or by compression. It comprises a mixture of active substances and excipients, usually in powder form, pressed or compacted from a powder into a solid dose. The excipients can include diluents, binders or granulating agents, glidants (flow aids) and lubricants to ensure efficient tabletting; disintegrants to promote tablet break-up in the digestive tract; sweeteners or flavours to enhance taste; and pigments to make the tablets visually attractive. A polymer coating is often applied to make the tablet smoother and easier to swallow, to control the release rate of the active ingredient, to make it more resistant to the environment (extending its shelf life), or to enhance the tablet's appearance.The compressed tablet is the most popular dosage form in use today. About two-thirds of all prescriptions are dispensed as solid dosage forms, and half of these are compressed tablets. A tablet can be formulated to deliver an accurate dosage to a specific site; it is usually taken orally, but can be administered sublingually, buccally, rectally or intravaginally. The tablet is just one of the many forms that an oral drug can take such as syrups, elixirs, suspensions, and emulsions. Medicinal tablets were originally made in the shape of a disk of whatever color their components determined, but are now made in many shapes and colors to help distinguish different medicines. Tablets are often stamped with symbols, letters, and numbers, which enable them to be identified. Sizes of tablets to be swallowed range from a few millimeters to about a centimeter.