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Over the Counter Pharmaceutical Formulations by David D. Braun Pdf
This book presents formulations for over-the-counter (OTC) or nonprescription drugs. The OTC drug formulations in this book are organized according to their therapeutic effect. There are 19 categories of OTC drugs included. Each category is presented in a single chapter that consists of two parts; Part I presents the composition of brand name products, and Part II presents starting or prototype formulations contributed by suppliers of raw materials for OTC drugs. The brand name products are listed alphabetically in Part I of each chapter, followed by the name of the manufacturer, the type and.
Handbook of Pharmaceutical Manufacturing Formulations by Sarfaraz K. Niazi Pdf
The fifth volume in the series, this book covers over-the-counter products, which include formulations of products classified by the US FDA under the OTC category. Each entry begins with a fully validated scaleable manufacturing formula and a summary of manufacturing process. The book provides a detailed discussion on the difficulties encountered in formulating and manufacturing OTC products. The section on regulatory and manufacturing guidance deals with the topics of cGMP practices for the OTC drug products, formulations of solid oral dosage forms, oral solutions and suspensions, validation of cleaning process, in addition to providing quick tips on resolving the common problems in formulating OTC drugs.
Handbook of Pharmaceutical Manufacturing Formulations by Sarfaraz K. Niazi Pdf
Pharmaceutical formulations remain as much an art today as they have evolved into complex science. With exponential growth of generic formulations, the need for ready formulations has increased. Essentially a cookbook for making drugs, the six-volume handbook contains the recipes and process steps for over 2000 drugs, including a number of biotechnology drugs. This first volume covers tablets, both coated and uncoated and oral powders. The author has painstakingly assembled this book from FDA New Drug Applications, patent applications and the BASF book of generic formulations, all supplemented by his 30-plus years of experience in pharmaceutical formulations.
Author : David B. Braun Publisher : William Andrew Page : 480 pages File Size : 53,9 Mb Release : 1994-12-31 Category : Medical ISBN : UOM:39015034866304
Over the Counter Pharmaceutical Formulations by David B. Braun Pdf
Each section contains brand name and supplier's formulations. Brand name sections include manufacturer, active ingredients and concentration and other ingredients. Supplier's section includes supplier, ingredients, and mixing procedure.
Handbook of Pharmaceutical Manufacturing Formulations by Sarfaraz K. Niazi Pdf
The fifth volume in the series, this book covers over-the-counter products, which include formulations of products classified by the US FDA under the OTC category. Each entry begins with a fully validated scaleable manufacturing formula and a summary of manufacturing process. The book provides a detailed discussion on the difficulties encountered in formulating and manufacturing OTC products. The section on regulatory and manufacturing guidance deals with the topics of cGMP practices for the OTC drug products, formulations of solid oral dosage forms, oral solutions and suspensions, validation of cleaning process, in addition to providing quick tips on resolving the common problems in formulating OTC drugs.
Handbook of Pharmaceutical Manufacturing Formulations by Sarfaraz Khan Niazi Pdf
The Handbook of Pharmaceutical Manufacturing Formulations, Third Edition: Volume Five, Over-the-Counter Products is an authoritative and practical guide to the art and science of formulating drugs for commercial manufacturing. With thoroughly revised and expanded content, this fifth volume of a six-volume set, compiles data from FDA and EMA new drug applications, patents and patent applications, and other sources of generic and proprietary formulations including author's own experience, to cover the broad spectrum of cGMP formulations and issues in using these formulations in a commercial setting. A must-have collection for pharmaceutical manufacturers, educational institutions, and regulatory authorities, this is an excellent platform for drug companies to benchmark their products and for generic companies to formulate drugs coming off patent.
Pharmaceutical Formulation by Geoffrey D Tovey Pdf
Formulation is a key step in the drug design process, where the active drug is combined with other substances that maximise the therapeutic potential, safety and stability of the final medicinal product. Modern formulation science deals with biologics as well as small molecules. Regulatory and quality demands, in addition to advances in processing technologies, result in growing challenges as well as possibilities for the field. Pharmaceutical Formulation provides an up to date source of information for all who wish to understand the principles and practice of formulation in the drug industry. The book provides an understanding of the links between formulation theory and the practicalities of processing in a commercial environment, giving researchers the knowledge to produce effective pharmaceutical products that can be approved and manufactured. The first chapters introduce readers to different dosage forms, including oral liquid products, topical products and solid dosage forms such as tablets and capsules. Subsequent chapters cover pharmaceutical coatings, controlled release drug delivery and dosage forms designed specifically for paediatric and geriatric patients. The final chapter provides an introduction to the vital role intellectual property plays in drug development. Covering modern processing methods and recent changes in the regulatory and quality demands of the industry, Pharmaceutical Formulation is an essential, up to date resource for students and researchers working in academia and in the pharmaceutical industry.
Over the Counter Pharmaceutical Formulations by David D. Braun Pdf
This book presents formulations for over-the-counter (OTC) or nonprescription drugs. The OTC drug formulations in this book are organized according to their therapeutic effect. There are 19 categories of OTC drugs included. Each category is presented in a single chapter that consists of two parts; Part I presents the composition of brand name products, and Part II presents starting or prototype formulations contributed by suppliers of raw materials for OTC drugs. The brand name products are listed alphabetically in Part I of each chapter, followed by the name of the manufacturer, the type and concentration of the active ingredient(s) and the product form(s). It is also customary, but not required, for the manufacturer to list the so-called ""inactive ingredients"" on the label of the product. Part II of each chapter (except chapter 17) includes starting formulations developed by a number of raw material suppliers. Those formulations that are included contain not only the concentration of the active ingredients but also the concentration of the other ingredients and, in most cases, a recommended procedure for mixing the formulation. This book includes 559 brand name formulations of 63 manufacturers and 270 suppliers' suggested formulations for a total of 829 formulations.
Handbook of Pharmaceutical Manufacturing Formulations by Safaraz K. Niazi Pdf
No other area of regulatory compliance receives more attention and scrutiny by regulatory authorities than the regulation of sterile products, for obvious reasons. With the increasing number of potent products, particularly the new line of small protein products, joining the long list of proven sterile products, the technology of manufacturing ster
Handbook of Pharmaceutical Additives by Michael Ash,Irene Ash Pdf
This handbook has been extensively updated and is available in either book or CD format (0-566-08505-4). It describes more than 5000 trade name and more than 3000 generic chemical components that are used in the formulation of both prescription and over-the-counter drugs. These additives enable or enhance the therapeutic delivery of the active ingredients in a variety of medications that include orals, topicals, suppositories, injectables, inhalants, etc.
Handbook of Pharmaceutical Additives by Michael Ash,Irene Ash Pdf
This Handbook of Pharmaceutical Additives describes more than 3,500 trade name products and 2,500 chemicals that function as pharmaceutical additives. Pharmaceutical additives are defined in this reference as the secondary ingredients that are present in both prescription and over-the-counter drug formulations and function to enable or enhance the delivery of the drug or medicine in a variety of dosage forms (i.e. oral - tablets, capsules, and liquid; topicals - dermal, ophthalmic, and otic; suppositories; injectables; respiratory; etc.). This definition of pharmaceutical additives encompasses excipients, inert or inactive ingredients, as well as synergists or chemicals that substantively contribute to the medicinal effects of the active ingredient.
Handbook of Pharmaceutical Manufacturing Formulations by Sarfaraz K. Niazi Pdf
The third volume in the six-volume Handbook of Pharmaceutical Manufacturing Formulations, this book covers liquid drugs, which include formulations of non-sterile drugs administered by any route in the form of solutions (monomeric and multimeric), suspensions (powder and liquid), drops, extracts, elixirs, tinctures, paints, sprays, colloidons, emul
Formulation Tools for Pharmaceutical Development by J E Aguilar Pdf
A range of new and innovative tools used for preformulation and formulation of medicines help optimize pharmaceutical development projects. Such tools also assist with the performance evaluation of the pharmaceutical process, allowing any potential gaps to be identified. These tools can be applied in both basic research and industrial environment. Formulation tools for pharmaceutical development considers these key research and industrial tools. Nine chapters by leading contributors cover: Artificial neural networks technology to model, understand, and optimize drug formulations; ME_expert 2.0: a heuristic decision support system for microemulsions formulation development; Expert system for the development and formulation of push-pull osmotic pump tablets containing poorly water-soluble drugs; SeDeM Diagram: an expert system for preformulation, characterization and optimization of tables obtained by direct compression; New SeDeM-ODT expert system: an expert system for formulation of orodispersible tablets obtained by direct compression; and 3D-cellular automata in computer-aided design of pharmaceutical formulations: mathematical concept and F-CAD software. Coverage of artificial intelligence tools, new expert systems, understanding of pharmaceutical processes, robust development of medicines, and new ways to develop medicines Development of drugs and medicines using mathematical tools Compilation of expert system developed around the world
An Introduction to Pharmaceutical Sciences by Jiben Roy Pdf
This textbook is written as a unified approach to various topics, ranging from drug discovery to manufacturing, techniques and technology, regulation and marketing. The key theme of the book is pharmaceuticals - what every student of pharmaceutical sciences should know: from the active pharmaceutical ingredients to the preparation of various dosage forms along with the relevant chemistry, this book makes pharmaceuticals relevant to undergraduate students of pharmacy and pharmaceutical sciences. This book explains how a particular drug was discovered and then converted from lab-scale to manufacturing scale, to the market. It explains the motivation for drug discovery, the reaction chemistry involved, experimental difficulties, various dosage forms and the reasoning behind them, mechanism of action, quality assurance and role of regulatory agencies. After having a course based on this book, the student will be able to understand: 1) the career prospects in the pharmaceutical industry, 2) the need for interdisciplinary teamwork in science, 3) the techniques and technology involved in making pharmaceuticals starting from bulk drugs, and 4) different dosage forms and critical factors in the development of pharmaceutical formulations in relation to the principles of chemistry. A few blockbuster drugs including atorvastatin, sildanefil, ranitidine, ciprofloxacin, amoxicillin, and the longest serving drugs such as aspirin and paracetamol are discussed in detail. Finally, the book also covers the important current pharmaceutical issues like quality control, safety, counterfeiting and abuse of drugs, and future prospects for pharmaceutical industry. Unified approach explaining drug discovery, bulk drug manufacturing, formulation of dosage forms, with pharmacological and therapeutic actions Manufacturing processes of representative active pharmaceutical ingredients and their chemistry plus formulation of dosage forms presented in this book are based on actual industrial processes Covers many aspects relevant to students of the pharmaceutical sciences or newly employed pharmaceutical researchers/employees. It contains summary information about regulatory agencies of different countries
