"Pharmaceutical formulation" Essays and Research Papers

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    Lack of bioequivalence between disulfiram formulations Exemplified by a tablet/effervescent tablet study Andersen‚ M. P. Lack of bioequivalence between disulfiram formulations. Acta Psychiatr Scand 1992: 86: 31-35. M. P. Andersen Pharmacokinetic Laboratory AIS Dumex (Dumex Ltd.)‚ DK-2300 Copenhagen Abstract - A comparison of the bioavailability of disulfiram (DSF) after administration of non-effervescent Antabusea tablets (CP Pharmaceuticals‚ UK) and Antabuse@effervescent tablets Antabus@(A/S

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    statement of purpose

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    ’a PhD in the field of Pharmaceutical Sciences’ - Statement of Purpose 1 of 4 http://www.essayforum.com/graduate-essays-4/phd-field-pharmaceutic... Ads not by this site EssayForum Unanswered [10] / Featured [1] / URGENT [0] help Log in Go or REGISTER NOW! Essay Forum / Graduate Essays / ’a PhD in the field of Pharmaceutical Sciences’ - Statement of Purpose nishantsg Nov 6‚ 2011‚ 10:07am #1 Statement of Purpose I am determined to pursue a PhD in the field

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    PHARMACEUTICALS

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    PHARMACEUTIC ALS INDUSTRY ANALYSIS GROUP MEMBERS: MANVI KARTHIKEYA VAMSI VINOD INDUSTRY ANALYSIS The Indian Pharmaceutical industry today is in the front rank of India’s science based industries with wide range capabilities in the complex field of drugs and technology. MARKET SIZE It ranks 4th in the world pertaining to the Volume of sales.  Estimated worth of Indian Pharmaceuticals Industry is US$ 6 billion  Almost 70% of domestic demand for bulk drugs is catered by Indian Pharma Industry

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    Zidovudine Case Study

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    optimization of formulation. The input variables chosen are amount of fenugreek mucilage‚ amount of mannitol‚ and concentration of PVP and the response parameters chosen for the optimization were Dissolution efficiency at 10 min and In-vitro dispersion

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    Formulation of Lamotrigine Orodispersible Tablets by Using New Generation Superdisintegrants B.Ramu 1*‚ N.Ramakrishna 2‚ B.Shivashanker3 1‚3 K.V.K College Of Pharmacy ‚ Department Of Pharmaceutics‚JNTUH Hyderabad India. 2 Avanthi institute of pharmaceutical sciences‚department of pharmaceutics Bandameedi.ramu@gmail.com ABSTRACT In the present work‚ an attempt has been made to develop fast disintegrating tablets of Lamotrigine. New generation super

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    Sci Research article Pharm www.scipharm.at Open Open Access Formulation Optimization of Hydrodynamically Balanced Oral Controlled Release Bioadhesive Tablets of Tramadol Hydrochloride Bhupinder SINGH *‚ Ashu RANI‚ BABITA‚ Naveen AHUJA‚ Rishi KAPIL University Institute of Pharmaceutical Sciences‚ UGC Center of Advanced Studies‚ Panjab University 160 014‚ Chandigarh‚ India. * Corresponding author. E-mail: bsbhoop@yahoo.com (B. Singh) Sci Pharm. 2010; 78: 303–323 Published: Accepted:

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    Pharmaceutical Industry

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    Laboratories ¬¬¬  Indian Pharmaceutical Industry can be valued at around $20billion (2009). By Volume‚ India is world’s second largest producer of pharmaceuticals‚ while by value it is world’s thirteenth largest. It is expected to grow at CAGR of 12% for 2010-2012 (global average 6%).Around 95% of Domestic demand is catered by Indian Pharmaceutical companies. In Indian Pharmaceuticals Market‚ Formulations accounted for 65% while Bulk Drugs accounted for 35% by Value. Formulations consist of Generic as

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    Pharmacy Sop

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    of the Indian Pharmaceutical Industry. With the signing of the General Agreement of Trade and Tariff and the World Trade Organization Treaty‚ India agreed to recognize both product and process patents. This made patented drugs with a modified process. Due to this‚ India has developed tremendous competitive edge in the manufacturing bulk drugs and formulations. These abundant opportunities with their challenges are where I see myself making a contribution to the Indian Pharmaceutical Industry and in

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    developed to increase gastric residence time and bioavailability after oral administration. Total six formulations were formulated by direct compression technique using varying concentrations of Kollidon SR (floating agent). The formulations were evaluated for their drug content‚ hardness‚ friability‚ buoyancy lag time‚ total floating time‚ swelling index and in­vitro drug release. All formulations possessed good floating properties with total floating time >12 hrs. Introduction & Objectives Oral

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    bioavailability compared to traditional tablets. Because of dispersion in saliva while still in the oral cavity‚ there can be pre-gastric absorption from some formulation in those cases where the drug dissolves quickly. Buccal‚ pharyngeal and gastric regions are all areas of absorption of the many formulations. However‚ other formulations show nearly identical plasma concentration profiles. Any pre-gastric absorption avoids first pass metabolism and can be a great advantage in drugs that undergo

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