Pharmacopoeias
please check current pricing due to the fluctuating dollar.. If you would like to order any of these, email balogh@balogh.com. The Japanese publishers have recently increased prices dramatically, so we had to increase prices on those publications.
NEW AND FORTHCOMING
German Homoeopathic Pharmacopoeia.
einschließl. 7. Akt.Lfg. 2011. Professionals engaged in all aspects of the
manufacture, evaluation, registration or dispensing of homoeopathic
substances or medicinal products now have access to a wealth of information
comprising 583 monographs and 286 general texts including reagents, vehicles
and excipients,analytical and the very important 54 manufacturing methods.
Homoeopathic and anthroposophical manufacturing methods are included as well
as the methods used in spagyrics and the production of organ-derived
preparations. The analytical methods have been harmonized with the European
Pharmacopoeia (Ph. Eur.) and the German Pharmacopoeia (DAB). Each monograph
is uniformly structured, listing (wherever applicable)
* origin
* description
* characteristics
* identification
* purity tests and
* assays
and providing information on the basic dosage forms and their
* manufacture
* characteristics
* identification
* purity tests
* assays and
* storage.
The loose-leaf format makes it easy for the user to keep his collection up
to date. ISBN 978-3-8047-5051-7. $620.00
Pharmacopoeia of the People's Republic of China 2010. August 2011. China Medical Science and Technology Press. Three Volumes containing herbs, plant oils and extracts, Narikata and single flavor preparations, a total of 2136 kinds of plants, including 990 new plants; includes chemicals, antibiotics, biochemical drugs, radioactive pharmaceuticals. Chinese Pharmacopoeia 2010 has been 69% revised, including ways to increase testing and higher standards. The new Pharmacopoeia seeks to cover the National Essential Drugs List species. Pharmacopoeia is divided into three volumes, containing 4567 received standard drugs. Volume 1 is for traditional Chinese medicine, sorting by English alphabetical order of pharmaceutical standards, Volume 2 contains chemicals, antibiotics, biochemical drugs and pharmaceutical excipients radioactive standard, sorting by English alphabetical order of generic API. Volume 3 contains biological products, sorting as its Chinese version. $1600.00
The British Pharmacopoeia (BP) 2012,
due August 2011. The BP 2012 is the leading collection of
standards for UK medicinal products and pharmaceutical substances, making it
an essential reference for anyone working within pharmaceutical research and
development, manufacture and testing.
The BP 2012 has been updated to include new
monographs and European Pharmacopoeia 7th edition text up to and including
Supplement 7.2.
The British Pharmacopoeia is different from
the European Pharmacopoeia in having British monographs (not incorporated into
the European Pharmacopoeia) as well as differences, in some cases, in dosage
forms and formulated preparations. In addition, many monographs carry additional
requirements from those of the European Pharmacopoeia.
Your BP 2012 package will include:
Six volume printed edition including the
BP (Veterinary) 2012;
Single-user licence to the CD-ROM
Online Subscription/CD-ROM: Following registration - using the ID code supplied with the hard copy - customers will be granted a single-user license to access the BP online and will have the option to receive the CD-ROM which contains the whole of the current British Pharmacopoeia. The CDROM which comes with the printed version must now be ordered by the customer themselves because of copyright infringement by some groups, click on this link to fill out the form and the cdrom will be mailed to you free of charge!
A concurrent user license allows maximum access through any workstation within an organization. This is essential for any organization that has several people wanting to access the vital information within BP 2011 simultaneously. Please inquire for more than 5 user licenses. 1-5 user license (includes 1 set of the printed version) will be $6260.00 shipping will be $50 due to high cost of insurance and shipping.
La Pharmacopée Française. 10th edition through 2010 supplements. Includes CDROM. This book defines the formal criteria of purity of raw materials used in the manufacture of drugs (human and veterinary) and analytical methods used to ensure their control. It is essential that all users of raw materials and pharmaceutical excipients, in charge of quality control and drug registration services. The French Pharmacopoeia 10th edition consists of three files updated in October 2010. They also include a list of medicinal plants and a cd-rom containing all monographs in pdf files in alphabetical order. $850.00
European Pharmacopoeia. 7th Edition due July 2010. Main volume 7.0 July, Supplement 7.1 October and Supplement 7.2 January. Instead of the DVD disk, there is a new USB Stick which is bilingual, you will be able to choose between the language options when you install the USB Stick. It will be possible to run the European Pharmacopoeia directly from any computer's USB port with no installation (after a one-time activation of the USB stick). As with the DVD previously, it will be possible to install the application onto 2 computers. ISBNs: Printed 978-92-871-6706-4; USB 978-92-871-6710-1. approximately $995 for the printed version or approximately $950 USB version (main plus 2 supplements).
Supplements 7.3-7.5: ISBN printed 978-92-871-6962-4, ISBN USB 978-92-871-6966-2. prices: printed for 3 supplements $799; for USB version $950 (The USB version normally comes out a month after the printed version)
- supplement 7.3 (published in June 2011 - new/revised texts agreed in November 2011 - for implementation in January 2012),
- supplement 7.4 (published in October 2011 - new/revised texts agreed in March 2011 - for implementation in April 2012), and
- supplement 7.5 (published in January 2012- new/revised texts agreed in June 2011- for implementation in July 2012).
Prices may change slightly due to the fluctuating dollar/euro.
.
Le
Dictionnaire VIDAL 2010. The 2010 VIDAL Drug Compendium. The reference for
drug information. 2010. The 86th edition
of the VIDAL Drug Compendium lists more than
5000 drugs and 4900 consumer
healthcare products, making it an essential reference for healthcare
professionals in their everyday practice. Each product monograph includes the
official prescription information provided in
the Summary of Product Characteristics (SPC) issued by the French
Health Products Safety Agency (Afssaps). The monographs are easy to reference
using an alphabetical listing by search category, and provide a complete
overview of the main features of each drug or product.
The 6 sections of the VIDAL Drug Compendium are color-coded, with an additional section providing practical information.
Alphabetical index of drug monographs.
Alphabetical index of personal care products divided into six categories (accessories, disinfection, nutrition, hygiene and cosmetics, reagents and tests, spas).
Alphabetical index of drugs by active ingredient (INN, FAN, or common nomenclature).
Drug classification by pharmacotherapeutic class.
Alphabetical directory of pharmaceutical companies and their products.
Generic drug index. in French only. 3200 pp. price $540.00
The Japanese Pharmacopoeia Fifteenth Edition. (JP XV). Official from March 31, 2007 . Edited by Society of Japanese Pharmacopoeia. 2007. The revised JP XV in English language comprises the following items in order: The Ministry of Health, Labour and Welfare Ministerial Notification; Contents; Preface; General Notices; General Rules for Crude Drugs; General Rules for Preparations; General Tests, Processes and Apparatus; Official Monographs, including Monographs for Crude Drugs; Infrared Reference Spectra; Ultraviolet-visual Reference Spectra; General Information; Atomic Weight Table (2004) and Standard Atomic Weights 2004 as Appendix ; and Cumulative Index (English, Latin and Japanese titles). Main features and revisions of this book are:
English and Latin titles of drugs were based on International Nonproprietary Names for Pharmaceutical Substances, and chemical names were based on Rules of International Union of Pure and Applied Chemistry (IUPAC). General Rules for Preparations which were revised are General Notices for Preparations; Extracts; Capsules; Transdermal Systems (new addition); Tablets; Injections; Plasters and Pressure Sensitive Adhesive Tapes; and Arrangements for others. In General Tests, Processes and Apparatus, “Content Uniformity Tests” and “Mass Variation Tests” were combined and renames as “Uniformity of Dosage Units”. General Tests, Processes and Apparatus which were revised are Ammonium Limit Test; Arsenic Limit Test; Crude Drugs Test; Disintegration Test; Dissolution Test; Insoluble Particulate Matter Test for Injections; Melting Point Determination; Microbial Assay for Antibiotics; Microbial Limit Test for Crude Drugs; Powder Particle Size Determination; Residue on ignition Test; Specified Surface Area Determination; and Test Methods for Plastic Containers, and which were deleted are Absorbance Ratio Method; Methoxyl Assay; Paper Chromatography, and Volatile Contaminations in Ethanol. Official Monographs provides 1483 articles, including 102 articles newly added and 8 articles deleted. 1820 pages, ISBN978-4-8408-0974-0 C3047, Hardbound, A4 format. $1400.00
Japanese Pharmacopoeia 15th edition supplement 1. October 2008. $600.00
Japanese Pharmacopoeia 15th edition, supplement 2. 2010. Official Monographs provides approx. 230 articles, including 106 articles newly added, 1 article deleted, 160 articles revised. General Tests, Process and Apparatus provides the following tests newly added: 2.04 Amino Acid Analysis of Proteins. Revision is made on the following 9 tests: 1.07 Heavy Metals Limit Test, 1.08 Nitrogen Determination (Semimicro-Kjeldahl Method), 1.09 Qualitative Tests, 2.01 Liquid Chromatography, 3.01 Determination of Bulk and Tapped Densities, 3.02 Specific Surface Area by Gas Adsorption, 3.03 Powder Particle Density Determination, 3.04 Particle Size Determination, 7.02 Test Methods for Plastic Containers. Addenda include the followings: The monographs revised in the Supplement II to JP 15th Edition and their revised sections, PMRJ Reference Standards Ordering Information for Foreign Users, PMRJ Reference Standards Catalog, PMRJ Order Form, and PMRJ Reference Standards User Information. p.p 312; A4 Format (210 x 297 mm); Paperback; ISBN978-4-8408-1135-4. $660.00
THE JAPANESE PHARMACEUTICAL CODEX 1997
Preface
General Notices
JPC 1997
Part I：Pharmaceutical Active Ingredients
PartII：Pharmaceutical Preparations
General Tests, Processes and Apparatus
（1）Reference Standards
（2）Reagents and Test Solutions
（3）Standard Solutions for Volumetric Analysis
（4）Standard Solutions
Index . 1848 pp. hardcover. English. $1500.00
The Japanese Cosmetic Ingredients Codex 1993 (JCIC 1993) plus supplement 1993. 1994; pp.1,000 plus supplement; B5 format (181x257 mm); hardback; ISBN4-8408-0308-0 C3047; Carries 1409 articles, comprising General Notices; General Tests, Processes and Apparatus; and Monographs, followed by Index. $1995.00
The
International Pharmacopoeia, Fourth Edition. World Health Organization (WHO).
2007. 'The International Pharmacopoeia - Fourth Edition' consolidates the texts
of the five separate volumes of the third edition. Certain additions and
amendments have been made to the notices in order to clarify the interpretation
of the Pharmacopoeia and to facilitate application of the requirements by the
user. This fourth edition will include all the monographs in the third edition
together with new monographs for didanosine, indinavir sulfate, nelfinavir
mesilate, nevirapine, ritonavir, saquinovir, saquinovir mesilate. All the
monograph texts are brought together in one section and the method texts in
another. Each of these major sections are divided into appropriate sub-sections
and the method texts are numbered for ease of cross-reference. Method texts that
have been updated include, for example, the text on high performance liquid
chromatography [HPLC]. This has been revised to clarify certain technical terms
and to add advice on adjustment of chromatographic conditions, as recommended by
the WHO Expert Committee on Specifications for Pharmaceutical Preparations in
October 2004. 924156301X; 9789241563017. $460.00
German Homoeopathic Pharmacopoeia. Professionals
engaged in all aspects of the manufacture, evaluation, registration or
dispensing of homoeopathic substances or medicinal products now have access to a
wealth of information comprising 583 monographs and 286 general texts including
reagents, vehicles and excipients, analytical and the very important 54
manufacturing methods. Homoeopathic and anthroposophical manufacturing methods
are included as well as the methods used in spagyrics and the production of
organ-derived preparations. The analytical methods have been harmonized with the
European Pharmacopoeia (Ph. Eur.) and the German Pharmacopoeia (DAB). Each
monograph is uniformly structured, listing (wherever applicable)
* origin
* description
* characteristics
* identification
* purity tests and
* assays
and providing information on the basic dosage forms and their
* manufacture
* characteristics
* identification
* purity tests
* assays and
* storage.
The loose-leaf format makes it easy for the user to keep his collection up to
date. 2008. 1994 p. 2 Ringbinders. Loose-leaf serial., ring binder.
ISBN 978-3-8047-5044-9. $680.00
MIMS Annual. 2010.
The MIMS Annual is the flagship product of MIMS Australia. It is this publication that has made MIMS the byword for accurate, reliable, comprehensive and independent medicines information. This has replaced the Australian Prescription Products Guide
The MIMS Annual is:
approximately $400 (depending on current exchange rate). hardcover, updated July of every year.
Prices may fluctuate with the Currency Exchange Rate!
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