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INDIAN PHARMACOPOEIA

In the United States, the first pharmacopoeia was published in December 1820 both in English and in Latin. Later on a National Formulary was also published in addition to U.S.P. (United States Pharmacopoeia). The object of the U.S.P.ws to select from substances the ones which possess medicinal power, converted them into preparation of suitable composition in order to enhance their power to the maximum advantage.

                           The first International Pharmacopoeia was published by the World Health Organization in 1951 (Volume I) and in 1955 (Volume II). The object of this was to provide a uniform list which would avoid the confusion caused by different national standards, strengths and names especially for the use of travelers who might need to use the same prescription in different countries.

First Edition of Pharmacopoeia of India
Fifth Edition of Pharmacopoeia of India
Third Edition of Pharmacopoeia of India
Fifth Edition of Pharmacopoeia of India

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Salient Features of the First Edition of Pharmacopoeia of India(1955)

The title of monographs have been given in Latin language. Abbreviated titles for use in prescription have been given immediately below the Latin title. The English title has also been given below the abbreviation title. The weights and measures have been given in metric system. All statements contained in the individual monographs have been considered as constitute standards for the official substances. Doses are expressed both in the metric system as well as in the English system. A list of preparations has been given at the end of some of the monographs. The temperature has been expressed in Celsius thermometric scale. The descriptive terms (very soluble, freely soluble, sparingly soluble, slightly soluble, very slightly soluble, practically insoluble) have been used where the exact solubility of a pharmacopoeial substance is not known. The tenure of the first Indian Pharmacopoeial Committee expired in 1954, and the Committee was reconstituted under the chairmanship of Dr. ...

HISTORY OF THE PHARMACOPOEIA OF INDIA

         The Government of India through its letter No. 2338 H(C)/43 dated 26 January, 1944, directed the Drugs Technical Advisory Board list the drugs used in India, which are not mentioned in British Pharmacopoeia and also recommend the standards to be prescribed to maintain uniformity and the chemical tests to be used to establish identity and purity. The Government of India published the Indian Pharmacopoeial List in 1946, as a supplement to the British Pharmacopoeia. The term “List” in the title was “misleading” in that, the book not only contained a list of drugs which were of substantial medicinal value but also laid down standards.                               The Indian Pharmacopoeial List contained about 180 monographs and a number of appendices prepared on the lines of...

Salient Features of the Fifth Edition of Pharmacopoeia of India(2007)

The Indian Pharmacopoeia 2007 is presented in three volumes. Volume I contains the general notes, preface, the structure of the IPC, Introduction and general chapters. Volume II deals with the general monographs on drug substances, dosage forms and pharmaceutical aids. Volume III contains monographs on drug substances, dosage forms, pharmaceutical aids, vaccines and immunosera for human use, herbs and herbal products, blood and blood related products, biotechnology products and veterinary products. General chemical tests for identification have been almost eliminated and more specific infrared and ultraviolet spectrophotometric tests have been given. The test for pyrogens involving the use of animals has been virtually eliminated. The test for bacterial endotoxins has been introduced. The test for abnormal toxicity is now confined to certain vaccines. The use of chromatographic methods has been extended in assays to large number of pharmaceutical products. 6. Labeling and storage ...