Over The Counter Pharmaceutical Formulations
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Author | : David B. Braun |
Publisher | : William Andrew |
Total Pages | : 480 |
Release | : 1994-12-31 |
Genre | : Medical |
ISBN | : |
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.
Author | : Geoffrey D Tovey |
Publisher | : Royal Society of Chemistry |
Total Pages | : 432 |
Release | : 2018-06-25 |
Genre | : Medical |
ISBN | : 1849739412 |
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.
Author | : Safaraz K. Niazi |
Publisher | : CRC Press |
Total Pages | : 458 |
Release | : 2016-04-19 |
Genre | : Medical |
ISBN | : 1420081314 |
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
Author | : David D. Braun |
Publisher | : |
Total Pages | : 568 |
Release | : 1994 |
Genre | : |
ISBN | : 9780080945965 |
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.
Author | : David D. Braun |
Publisher | : William Andrew |
Total Pages | : 472 |
Release | : 2012-12-02 |
Genre | : Technology & Engineering |
ISBN | : 0815518498 |
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.
Author | : J E Aguilar |
Publisher | : Elsevier |
Total Pages | : 304 |
Release | : 2013-09-30 |
Genre | : Medical |
ISBN | : 1908818506 |
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
Author | : Thorsteinn Loftsson |
Publisher | : Academic Press |
Total Pages | : 170 |
Release | : 2014-01-25 |
Genre | : Medical |
ISBN | : 0124115624 |
Drug Stability for Pharmaceutical Scientists is a clear and easy-to-follow guide on drug degradation in pharmaceutical formulation. This book features valuable content on both aqueous and solid drug solutions, the stability of proteins and peptides, acid-base catalyzed and solvent catalyzed reactions, how drug formulation can influence drug stability, the influence of external factors on reaction rates and much more. Full of examples of real-life formulation problems and step-by-step calculations, this book is the ideal resource for graduate students, as well as scientists in the pharmaceutical and related industries. - Illustrates important theoretical concepts with numerous examples, figures, calculations, learning problems and questions for self-study and retention of material - Provides answers and explanations to test your knowledge - Enables you to better understand key concepts such as rate and order of reaction, reaction equilibrium, complex reaction mechanisms and more - Includes an in-depth discussion of both aqueous and solid drug solutions and contains the latest international regulatory requirements on drug stability
Author | : Vitthal S. Kulkarni |
Publisher | : Academic Press |
Total Pages | : 256 |
Release | : 2015-10-15 |
Genre | : Science |
ISBN | : 012801072X |
A needed resource for pharmaceutical scientists and cosmetic chemists, Essential Chemistry for Formulators of Semisolid and Liquid Dosages provides insight into the basic chemistry of mixing different phases and test methods for the stability study of nonsolid formulations. The book covers foundational surface/colloid chemistry, which forms the necessary background for making emulsions, suspensions, solutions, and nano drug delivery systems, and the chemistry of mixing, which is critical for further formulation of drug delivery systems into semisolid (gels, creams, lotions, and ointments) or liquid final dosages. Expanding on these foundational principles, this useful guide explores stability testing methods, such as particle size, rheological/viscosity, microscopy, and chemical, and closes with a valuable discussion of regulatory issues. Essential Chemistry for Formulators of Semisolid and Liquid Dosages offers scientists and students the foundation and practical guidance to make and analyze semisolid and liquid formulations. - Unique coverage of the underlying chemistry that makes possible stable dosages - Quality content written by experienced experts from the drug development industry - Valuable information for academic and industrial scientists developing topical and liquid dosage formulations for pharmaceutical as well as skin care and cosmetic products
Author | : Mitchell J. Stoklosa |
Publisher | : |
Total Pages | : 428 |
Release | : 1986 |
Genre | : Medical |
ISBN | : 9780812110074 |
Author | : Sarfaraz K. Niazi |
Publisher | : CRC Press |
Total Pages | : 258 |
Release | : 2004-04-27 |
Genre | : Medical |
ISBN | : 1420048457 |
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