BP102T • General Pharmacy • Topic 1

History of Pharmacy, Pharmacopoeias & Prescriptions

Welcome to Topic 1 of General Pharmacy (BP102T). This lecture guide covers the entire official syllabus heading-by-heading: the history of pharmacy in India (education, industry, organizations), the scope of the pharmacy profession, official pharmacopoeias (IP, BP, USP, BPC, Int. Ph, NFI), study of a model IP monograph, parts of a prescription, how to handle prescriptions, and common Latin medical terms.

1. History of Pharmacy in India in Relation to Pharmacy Education

Simple Definition:

Pharmacy is defined as the health science that links medical science with chemistry. It is responsible for the discovery, production, control, disposal, and safe and effective use of medications.

  • • It is also known as: The profession of compounding and dispensing medicines.
  • • Pharmacy Education in India: Introduced in 1932 by Prof. M. L. Schroff (revered as the Father of Pharmacy Education in India) at Banaras Hindu University (BHU).
  • • Pharmacy Council of India (PCI): Constituted under the Pharmacy Act 1948 to regulate pharmacy qualifications and education standards across India.

In ancient times, medicine knowledge was passed down through the Guru-Shishya parampara using classical Ayurvedic texts like Charaka Samhita and Sushruta Samhita. There were no separate pharmacy colleges.

During the early British period, compounders and dispensers received only basic apprentice training in hospitals without any scientific syllabus. The systematic growth of pharmacy education happened through the following major milestones:

Milestone 1: The Chopra Committee (1930)

The British Government appointed the Drugs Enquiry Committee under the chairmanship of Col. R. N. Chopra. The committee pointed out that India had no trained pharmacists and strongly recommended starting university-level pharmacy degree courses.

Milestone 2: Prof. M. L. Schroff & Banaras Hindu University (1932)

Prof. Mahadeva Lal Schroff is revered as the "Father of Pharmacy Education in India". In 1932, he introduced pharmacy as a subject at Banaras Hindu University (BHU), and in 1937, he launched the very first 3-year Bachelor of Pharmacy (B.Pharm) degree course in India. Later, he also initiated M.Pharm education in 1940.

Milestone 3: The Pharmacy Act (1948) & Education Regulations

The Government enacted the Pharmacy Act in 1948 to regulate education. Under this act, the Pharmacy Council of India (PCI) was constituted in 1949. The PCI framed the Education Regulations (ER), which prescribed the minimum standards for the Diploma in Pharmacy (D.Pharm) and Degree (B.Pharm) across the country.

Milestone 4: Introduction of Doctor of Pharmacy (Pharm.D) & Modern Courses

In 2008, PCI introduced the 6-year clinical Pharm.D (Doctor of Pharmacy) program to prepare pharmacists for direct hospital patient care. Under the National Education Policy (NEP 2020) and the PCI 2026 Curriculum, pharmacy education now integrates computer programming (Python), data analytics, and modern clinical skills.

2. History of Pharmacy in India in Relation to Pharmaceutical Industries

Before the 20th century, almost 100% of allopathic medicines sold in India were imported from England, Germany, and France. India had no domestic drug industry. The growth of the Indian pharmaceutical industry can be understood in four phases:

Phase 1: Pioneers (1901 – 1947)

Birth of Indigenous Manufacturing

• 1901: Acharya Prafulla Chandra Ray established Bengal Chemical and Pharmaceutical Works in Calcutta, the very first modern pharmaceutical factory in India.
• 1907: Prof. T.K. Gajjar and B.D. Amin founded Alembic Chemical Works at Baroda to manufacture spirituous medicines.
• Small units like Bengal Immunity (1919) were established to make vaccines and sera.

Phase 2: Post-Independence (1947 – 1970)

Public Sector Leadership

The Government of India set up public sector units to produce affordable life-saving medicines:
• Hindustan Antibiotics Limited (HAL) in 1954 at Pimpri (Pune) to make Penicillin.
• Indian Drugs and Pharmaceuticals Limited (IDPL) in 1961 to manufacture synthetic bulk drugs and antibiotics.

Phase 3: The Indian Patent Act (1970)

The Generic Revolution

The Patents Act 1970 allowed process patents instead of product patents for medicines. This allowed Indian scientists to develop new, cost-effective chemical routes (reverse engineering), giving rise to private pharma giants like Ranbaxy, Cipla, Dr. Reddy's, Lupin, and Sun Pharma.

Phase 4: Global Leader (Present Era)

"Pharmacy of the World"

Today, India ranks 3rd globally by production volume and 14th by value. India supplies over 20% of global generic drugs, over 60% of world vaccines (Serum Institute of India, Bharat Biotech), and has the largest number of US FDA-approved pharmaceutical plants outside the United States.

3. History of Pharmacy in India in Relation to Pharmaceutical Organizations

Professional organizations protect the rights of pharmacists, maintain ethics, set education standards, and represent India on international platforms. Here are the premier pharmaceutical organizations in India:

OrganizationFull FormYear FoundedKey Role & Contribution
IPAIndian Pharmaceutical Association1939Founded by Prof. M.L. Schroff. It is the premier association of pharmacists in India, represents India at the International Pharmaceutical Federation (FIP), and publishes the Indian Journal of Pharmacy.
PCIPharmacy Council of India1949Statutory apex body under the Ministry of Health. Regulates pharmacy education, inspects and approves colleges, and maintains the Central Register of Pharmacists.
CDSCOCentral Drugs Standard Control Organization1971Headed by the Drugs Controller General of India (DCGI). Regulates drug approvals, clinical trials, import licenses, and sets standards under the Drugs and Cosmetics Act.
IHPAIndian Hospital Pharmacists Association1963Promotes hospital pharmacy practice, patient safety, hospital drug store management, and publishes the Indian Journal of Hospital Pharmacy.
APTIAssociation of Pharmaceutical Teachers of India1966Dedicated to pharmacy teachers, advancing teaching pedagogy, research grants, and curriculum development.
IPGAIndian Pharmacy Graduates' Association1973Unites degree-holding pharmacy graduates, works for career advancement, and advises government on pharmacy policy.
IPCIndian Pharmacopoeia Commission2005 (Autonomous)Headquartered at Ghaziabad. Publishes the Indian Pharmacopoeia (IP), National Formulary of India (NFI), and manages the Pharmacovigilance Programme of India (PvPI).

4. Scope of the Pharmacy Profession: Roles and Responsibilities

Scope of the Pharmacy Profession Infographic
Figure: Scope and Career Pathways of the Pharmacy Profession

A. Community / Retail Pharmacy

• Dispensing: Accurately checking and dispensing prescription medicines.
• Patient Counseling: Explaining dose, frequency (before/after food), and side effects.
• Storage & Inventory: Maintaining cold chain (2°C to 8°C) for vaccines and insulin.
• Health Screening: Monitoring blood pressure, blood glucose, and advising on OTC medicines.

B. Hospital & Clinical Pharmacy

• Inpatient Dispensing: Supplying medicines to ICU and ward patients.
• Compounding: Preparing sterile IV admixtures and total parenteral nutrition (TPN).
• Clinical Rounds: Working alongside doctors, checking drug-drug interactions.
• TDM: Therapeutic Drug Monitoring for narrow index drugs (Digoxin, Phenytoin).

C. Industrial Pharmacy & R&D

• Formulation & R&D: Designing new tablets, syrups, and drug delivery systems.
• Production: Manufacturing batches following Current Good Manufacturing Practices (cGMP).
• QC & QA: Testing raw materials, packaging, and finished products in labs.
• Regulatory Affairs: Filing drug dossiers (CTD format) with CDSCO and US FDA.

5. Pharmacopoeias & Official Books

Simple Definition:

A Pharmacopoeia is defined as an official book published by the authority of a government containing a list of medicines, their descriptions, purity tests, formulas, and legal standards.

1. Indian Pharmacopoeia (IP)
  • • It is also known as: The official drug book of India (IP).
  • • It is used for: Setting legal standards of identity, purity, and strength for all medicines manufactured and sold in India.
  • • Published by: The Indian Pharmacopoeia Commission (IPC), Ghaziabad under the Drugs and Cosmetics Act 1940.
2. British Pharmacopoeia (BP)
  • • It is also known as: The UK national pharmacopoeia (BP).
  • • It is used for: Providing statutory standards for pharmaceutical ingredients and medicines in the United Kingdom and Commonwealth nations.
3. United States Pharmacopeia (USP-NF)
  • • It is also known as: The American official drug compendium.
  • • It is used for: Specifying legal standards in the USA; USP sets standards for active drug substances (APIs), while the National Formulary (NF) sets standards for pharmaceutical excipients.
4. British Pharmaceutical Codex (BPC)
  • • It is also known as: The dispenser's reference manual.
  • • It is used for: Formulating, preparing, and compounding extemporaneous medicines in pharmacies and hospital dispensaries.
5. International Pharmacopoeia (Ph. Int.)
  • • It is also known as: The WHO global pharmacopoeia.
  • • It is used for: Creating uniform global quality specifications for priority essential medicines and orphan drugs worldwide.
6. National Formulary of India (NFI):

Published by IPC Ghaziabad; guides doctors and pharmacists on rational medicine use, dosage, and side effect management.

6. Structure and Content of the Indian Pharmacopoeia (IP)

Modern editions of the Indian Pharmacopoeia (such as IP 2018 / IP 2022) are published in 4 volumes:

  • Volume I: Notice, Preface, Introduction, General Notices, and General Chapters (apparatus, dissolution testing, chromatography HPLC/GC, and microbial assay methods).
  • Volume II: General Monographs on Active Pharmaceutical Ingredients and dosage forms (Letters A to F).
  • Volume III: General Monographs on Active Pharmaceutical Ingredients and dosage forms (Letters G to P).
  • Volume IV: Monographs (Letters Q to Z), Vaccines, Immunosera, Blood products, Herbal medicines, and Veterinary monographs.

Indian Pharmacopoeia Editions Timeline (1955 to 2022):

EditionYearChairman / AuthorityVolumesCover Color
1st Edition1955Dr. B. N. Ghosh1 VolumeBrown
2nd Edition1966Dr. B. Mukherjee1 VolumeRed
3rd Edition1985Dr. Nityanand2 VolumesBlue
4th Edition1996Dr. Nityanand2 VolumesLight Green
5th Edition2007IPC (Ghaziabad)3 VolumesDark Blue
6th Edition2010IPC (Ghaziabad)3 VolumesDark Green
7th Edition2014IPC (Ghaziabad)4 VolumesDeep Blue
8th Edition2018IPC (Ghaziabad)4 VolumesOrange
9th Edition2022IPC (Ghaziabad)4 VolumesOrange / Blue

7. Study of One Model IP Monograph: Paracetamol IP

A Monograph is defined as a complete official technical sheet for one specific drug in the pharmacopoeia. Here is the model monograph of Paracetamol IP:

MODEL IP MONOGRAPH: PARACETAMOL IPOfficial Standard
1. Official Title & Synonyms:PARACETAMOL IP (Acetaminophen, 4-Acetamidophenol). Chemical formula: C₈H₉NO₂. Molecular weight: 151.2 g/mol.
2. Category:Analgesic (pain reliever) and Antipyretic (fever reducer).
3. Purity Statement (Assay):Paracetamol contains not less than 99.0% and not more than 101.0% of C₈H₉NO₂ calculated on the dried basis.
4. Description:White, crystalline powder; odorless; slightly bitter taste.
5. Solubility:Sparingly soluble in cold water; freely soluble in boiling water; freely soluble in 95% alcohol.
6. Identification Tests:• Test A (IR spectrum): Spectrum matches Paracetamol Reference Standard.
• Test B (Color test): Boil 0.1 g with hydrochloric acid, add water, cool, add potassium dichromate; a violet color develops.
7. Melting Point Range:Between 168°C to 172°C.
8. Storage:Store protected from light and moisture in tightly closed containers.

8. Introduction to Prescription: Structure & Parts

Simple Definition:

A Prescription is defined as a written order from a registered medical practitioner (physician, dentist, or veterinarian) to a pharmacist to compound and dispense a specific medication for an individual patient.

  • • It consists of: 8 standard parts: Date, Patient Info, Superscription (℞), Inscription (drug names and doses), Subscription (pharmacist directions), Signatura (patient directions), Refill info, and Doctor's Signature.
  • • It is used for: Ensuring accurate dispensing, patient safety, and legal accountability of therapeutic drugs.
Prescription Guide Clipboard Infographic
Figure: Systematic Parts and Structure of a Prescription

Simple Definition:

A Prescription is defined as a legal written order from a registered medical practitioner (doctor) to a registered pharmacist asking to prepare and dispense specific medicines to a patient.

The 8 Systematic Parts of a Prescription:

  1. 1. Prescriber's Information & Date: Doctor's name, qualification, clinic address, and date of writing. Date prevents illegal misuse of old prescriptions.
  2. 2. Patient's Information: Patient name, age, sex, weight, and address. Age and body weight are needed to calculate correct pediatric or geriatric doses.
  3. 3. Superscription (Rx):
    • • It is also known as: The heading of the prescription (symbol Rx).
    • • It is used for: Commencing the prescription, originating from the Latin word Recipe, meaning "Take thou" (you take this medicine).
  4. 4. Inscription (The Main Body):
    • • It is also known as: The core formula or body of the prescription.
    • • It is used for: Listing the exact names, active ingredients, and dosage strengths of the medicines (for example, Tab. Paracetamol 500 mg).
  5. 5. Subscription: Directions to the pharmacist on what dosage form to prepare and how many units to dispense (e.g., "Dispense 10 capsules").
  6. 6. Signatura (Sig.): Instructions for the patient on how to take the medicine (e.g., "Take 1 tablet twice a day after meals").
  7. 7. Refill Instructions: Mentions whether the patient can purchase the medicine again without a fresh doctor visit.
  8. 8. Signature & Registration Number: Doctor's legal signature and state medical council registration number.

9. Handling of Prescriptions (Step-by-Step Procedure)

In this method, the pharmacist performs 4 systematic steps: Receiving, Reading and checking, Compounding and packaging, and Delivering with clear patient counseling.

When a prescription arrives at the pharmacy counter, the pharmacist must follow these 5 standard steps:

1
ReceivingReceive personally with a calm, polite face.
2
ReadingRead carefully; check doctor signature and date.
3
CheckingCheck dose, frequency, and drug interactions.
4
CompoundingWeigh accurately and pack in clean containers.
5
DeliveringExplain dosage instructions to the patient.

10. Latin Terminology Related to Prescriptions

Doctors use short Latin words on prescriptions. Here is the essential table every pharmacy student must know:

Latin PhraseAbbreviationEnglish Meaning
Semel in dieo.d. / s.i.d.Once a day
Bis in dieb.i.d.Twice a day
Ter in diet.i.d.Three times a day
Quater in dieq.i.d.Four times a day
Statimstat.Immediately (right now)
Pro re natap.r.n.As needed / when required
Ante cibosa.c.Before food / before meals
Post cibosp.c.After food / after meals
Hora somnih.s.At bedtime
Omni maneo.m.Every morning
Omni nocteo.n.Every night
Guttaegutt.Drops
Capsulacap.A capsule
Tabellatab.A tablet
Unguentumung.An ointment
Misturamist.A mixture
Fiatft.Make / let it be made
Quantum sufficiatq.s.As much as needed (sufficient quantity)