February 22, 2024

Salient features of Indian Pharmacopoeia

Salient features of Indian Pharmacopoeia

The actual process of publishing the first Pharmacopoeia started in the year 1944 under the chairmanship of Col. R. N. Chopra. The I. P. list was first published in the year 1946 and was put forth for approval. The titles are suffixed with the respective years of publication, e.g. IP 1996.

Salient features of Indian Pharmacopoeia 2018 include

  • General Chemical tests and TLC for identification of an article have been almost eliminated and more specific infrared, ultraviolet spectrophotometer and HPLC tests have been given emphasis.
  • The use of chromatographic methods has been greatly extended to cope with the need for more specificity in assays and in particular, in assessing the nature and extent of impurities in ingredients and products.
  • Most of the existing Assays and Related Substances Test methods are upgraded by liquid chromatographic technique in view to harmonizing with other International Pharmacopoeia.
  • Pyrogen tests have been replaced by Bacterial Endotoxin tests (BET) in parenteral preparations and other monographs
  • 53 New Fixed-Dose Combination (FDC) combination monographs have been included, out of which 25 FDC monographs are not available in any Pharmacopoeia.
  • General Chapters on Volumetric Glassware, Conductivity, Dissolution test, Disintegration test, Dimensions of Hard Gelatin Capsule Shells etc. have been revised.
  • For Controlling the Microbial quality of all the medicinal products general chapter on
  • Maintenance, Identification, Preservation and Disposal of Microorganism have been revised.

New Additions

• 170 Chemical Monographs

15 Herbal Monographs

Blood and Blood-related products: 10 Monographs

6 Monographs on Biotechnology derived therapeutic products

Radiopharmaceuticals: 3 Monographs

2 Monographs on Vaccines and Immunosera for Human use

14 Monographs on Veterinary Non Biologicals

The Indian Pharmacopoeia (IP) is the official document that defines the standards for drugs in India. It contains detailed information on the quality, purity, and potency of medicines available in the country. Some of the salient features of the Indian Pharmacopoeia are:

  1. Comprehensive Monographs: The IP contains monographs on various drugs, including their chemical structure, physical characteristics, and methods of analysis.
  2. Quality Standards: The IP sets the quality standards for medicines, including their active ingredient content, impurities, and packaging requirements.
  3. Evidence-based Approach: The IP uses the latest scientific data and research to establish its standards and guidelines.
  4. User-friendly Format: The IP is designed to be user-friendly, with clear and concise information presented in an easy-to-read format.
  5. Regular Updation: The IP is regularly updated to ensure that it reflects the latest scientific advancements and changes in the industry.
  6. Legal Recognition: The IP is legally recognized in India and its standards are enforced by the regulatory authorities.
  7. Essential for Licensing: The IP is an essential reference for manufacturers, suppliers, and regulators of medicines, as compliance with its standards is a requirement for licensing and selling drugs in India.

In conclusion, the Indian Pharmacopoeia plays a crucial role in ensuring the quality, safety, and efficacy of drugs in India, and is an important tool for the pharmaceutical industry, regulatory authorities, and healthcare professionals.

Editions of Indian Pharmacopoeia

EditionYearVolumesAddendum/Supplement
1st Edition1955Supplement 1960
2nd Edition1966Supplement 1975
3rd Edition19852Addendum 1989
Addendum 1991
4th Edition19962Addendum 2000
Vet Supplement 2000
Addendum 2002
Addendum 2005
5th Edition20073Addendum 2008
6th Edition20103Addendum 2012
7th Edition20144Addendum 2015
Addendum 2016
8th Edition20184Addendum 2019
Addendum 2021

Read more about What is Pharmacopoeia? What is International Pharmacopoeia?


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IPC Nagpur

First Year B Pharmacy Syllabus

B Pharmacy Subjects List for F Y B Pharm include following Theory and Lab

Semester I

Theory

BP101T Human Anatomy and Physiology I Theory
BP102T Pharmaceutical Analysis I Theory
BP103T Pharmaceutics I Theory
BP104T Pharmaceutical Inorganic Chemistry Theory
BP105T Communication skills Theory *
BP106RBT Remedial Biology
BP106RMT Remedial Mathematics Theory*

Practical

BP107P Human Anatomy and Physiology Practical
BP108P Pharmaceutical Analysis I Practical
BP109P Pharmaceutics I Practical
BP110P Pharmaceutical Inorganic Chemistry Practical
BP111P Communication skills Practical*
BP112RBP Remedial Biology Practical*

Semester II

Theory

BP201T Human Anatomy and Physiology II – Theory
BP202T Pharmaceutical Organic Chemistry I – Theory
BP203T Biochemistry – Theory
BP204T Pathophysiology – Theory
BP205T Computer Applications in Pharmacy – Theory *
BP206T Environmental sciences – Theory *

Practical

BP207P Human Anatomy and Physiology II Practical
BP208P Pharmaceutical Organic Chemistry I Practical
BP209P Biochemistry Practical
BP210P Computer Applications in Pharmacy Practical