and Tablets
FORMULATION AND EVALUATION OF ORAL DISINTEGRATING TABLETS OF URAPIDIL
... disintegrating tablets are also called as orodispersible tablets, quick disintegrating tablets, mouth dissolving tablets, fast disintegrating tablets, fast dissolving tablets, ...
15
Formulation development and evaluation of rapidly disintegrating antacid tablets
... Aluminum hydroxide is an effective oral antacid. It is available in form of dried aluminum hydroxide gel consist largely of hydrated aluminium oxide together with varying quantities of basic aluminium carbonate & ...
5
“Formulation Development and Evaluation of Atorvastatin Calcium Tablets Using Co-Processed Excipients” by Madhur Chandrashekhar Kulkarni, Sunil Vitthalrao Kolhe, India.
... 7. In- vitro drug release study – were undertaken using USP Dissolution apparatus type II (Electrolab Model No: TDT- 06L). The tablets containing 40 mg of Atv were added to the dissolution flasks containing 900ml ...
6
Use of thin layer chromatography to detect counterfeit sulfadoxine/pyrimethamine tablets with the wrong active ingredient in Malawi
... of tablets of types X and Y, the sample Z showing chip- pings, and eight further, randomly selected ...respectively, tablets of type X showed a peak at 3.43 min (paracetamol), and tablets of type Y ...
7
“A Brief Review on Oro-Dispersible Tablets: A Popular Growing Technology” by V.Nagesh, Gowtham kumar Vangala, Riddesh Sahoo, Ajey Kumar Reddy T, C.Haranath, C.Sowmya, India.
... In an survey conducted in Norway; among 6158 GP patients, approximately 26% patients reported that they do not take their prescribed medication as they had encountered problems in swallowing the conventional ...
12
Formulation and Evaluation of Simvastatin Floating Tablets
... 20 tablets which was performed in the study from each formulation remained within + 5 ...the tablets tested during the friability test was considered acceptable and any broken or smashed tablets were ...
6
DEVELOPMENT AND BIOEQUIVALENCE STUDY OF OLANZAPINE 10mg TABLETS
... mg Tablets was within the acceptable limits of the United States Pharmacopoeial ...mg Tablets had a good dissolution ...mg Tablets fall well within the proposed stability ...
6
Formulation and in vitro characterization of tapentadol HCL as immediate release tablets
... The content of drug was carried out by five randomly selected tablets of each formulation. The five tablets were grinded in mortar to get powder, this powder was dissolved in pH 6.8 phosphate buffer by ...
7
Design, prepare and evaluation of terbutaline tablets for chrono modulated pulsatile drug delivery system
... of tablets to the combined effect of abrasion and shock by utilizing a plastic chamber that revolves at 25 rpm dropping the tablets at distance of 6 inches with each ...Twenty tablets were weighed ...
10
FORMULATION AND EVALUATION OF LAMIVUDINE AND TENOFOVIR DISPROXIL FUMARATE IR TABLETS
... the tablets to disintegrate and pass through the mesh was ...Twenty tablets were selected at random and their average weight was determined using an electronic balance (Shimadzu Aux200, ...The ...
5
Formulation and evaluation of simvastatin buccal adhesive tablets
... adhesive tablets of Simvastatin that could be applied to the buccal mucosa to release the drug unidirectionally in buccal cavity in order to decrease gastric irritation and avoid first pass effect for improvement ...
10
Formulation and evaluation of bisoprolol fumarate extended release tablets
... The In –vitro dissolution studies were performed for all the formulation of tablets including commercial formulation using USP II tablet dissolution tester employing Paddle type at 100 rpm using 900 ml. of 6.8 pH ...
22
“Formulation and Evaluation of Allium sativum Tablets for Improved Oral Delivery” by Onyechi J.O., Chime S.A., OnyishiI.V., Brown S.A., Eleigwe P.O., Onunkwo G.C., Nigeria.
... in tablets weight will lead to variation in drug content which could also affect the overall bioavailability of the ...of tablets weight uniformity test are shown in Table 2, from the values obtained, the ...
5
Formulation of Glipizide Time-Controlled Release Tablets By Press Coating Using Hydrophilic and Hydrophobic Polymers – Its In Vitro Dissolution, Time Lag and Kinetic Models
... GLIPIZIDE TIME-CONTROLLED RELEASE TABLETS BY PRESS COATING USING HYDROPHILIC AND HYDROPHOBIC POLYMERS – ITS IN VITRO DISSOLUTION, TIME LAG AND KINETIC MODELS” was carried out by S. CHAITANYA KUMAR, in the ...
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FORMULATION, DEVELOPMENT AND IN-VITRO EVALUATION OF ORODISPERSIBLE TABLETS OF LAMOTRIGINE
... compliance. Tablets and capsules are popular solid dosage ...swallowing tablets and hard gelatin capsules, called ...Orodispersible tablets are also called as orally disintegrating tablets, ...
12
FORMULATION AND EVALUATION OF FAST DISINTEGRATING TABLETS OF VALSARTAN BY USING BANANA POWDER AS DISINTEGRATING AGENT
... disintegrating tablets of Valsartan by using Banana powder and SSG with different concentrations 2%, 4%, 6%, individually by using different diluents like Mannitol and Microcrystalline cellulose by direct ...
10
Mouth Dissolving Tablets Highlighting Innovative Techniques and Use of Natural Super disintegrant a concise review
... The formulations contained hydrolyzed and unhydrolyzed gelatin as a supporting specialists for the lattice, mannitol as a building operators and sodium starch glycolate/croscaramellose as a disintegrant. Breaking down ...
10
Mouth Dissolving Tablets-Pediatric and Geriatric Patient Compliance Dosage Forms
... dissolving tablets are novel approach under a solid oral drug delivery ...dissolving tablets are a convenience to all age group patients ( includes pediatrics, geriatrics ) psychotic ...dissolving ...
5
A Review on Oro-Dispersible Doxycycline Tablets
... form tablets. Most pharmaceutical tablets are processed by wet granulation, and yet it is the most complex means of tablet ...producing tablets, and for low dose drugs the granulation process is seen ...
11
Formulation Development and In-Vitro Evaluation of Potassium Chloride Extended Release Tablets
... strong tablets with 200 to 300 N crushing strengths can be produced, and these tablets will disintegrate within five minutes or less using the super- ...
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