Japanese Pharmacopoeia (JP) is established and published to regulate the properties and quality of drugs by the Minister of Health, Labour and Welfare after hearing the opinion of the Pharmaceutical Affairs and Food Sanitation Council (PAFSC).
The JP consists of General Notices, General Rules for Crude Drugs, General Rules for Preparations, General Tests, Processes and Apparatus and Official Monographs.
Items selected for entry in the JP must be those important in health care based on the necessity of the drug in medical practice, wide application and experience of use.
Since it was first published in June 1886, the JP has been revised many times periodically. The 16th edition of the JP came into effect on April 1, 2011.
The Japanese Pharmacopoeia 16th edition
The 16th edition (Determination of Bulk and Tapped Densities, Bacterial Endotoxins Test)(PDF:372KB)
The 16th edition
Table of errata(PDF:498KB)
Supplement I of the 16th edition
Table of errata(PDF:85KB)
Uniformity of Dosage Units and Monographs on Gelatin (PDF:409KB)
Supplement ＩＩ of the 16th edition
The Japanese Pharmacopoeia 15th edition
The 15th edition
Table of errata(PDF:917KB)
Supplement I of the 15th(PDF:4,424KB)
Monographs on Glycerin and concentrated Glycerin (PDF:101KB)
Microbiological Examination of the Non-sterile Products, Sterility Test, Disintegration Test and Dissolution Test (PDF:644KB)
Monographs on Heparin Sodium and Heparin Calcium (PDF:175KB)
Monographs on Longgu and Powdered Longgu (PDF:125KB)
Supplement II of the 15th（PDF:5,564KB）
The Japanese Pharmacopoeia 14th edition
The 14th edition
Supplement 1 of the 14th edition
Supplement 2 of the 14th edition
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