BTEUP D.Pharm 1st Year Final Exam — Predicted Questions
Subject: Pharmacy
BTEUP D.Pharm 1st Year Final Exam: Predicted Questions (ER-2020 Syllabus) Chapter-wise | Maximum 20 Questions per Subject Important Note for Students : This list contains highly likely questions based on an in-depth analysis of BTEUP previous year papers (2022-2025), syllabus importance, and exam trends. Use these questions to focus your study and revision. They are a valuable guide, but always supplement with your full course material for comprehensive preparation. SUBJECT 1: PHARMACEUTICS (ER20-11T) Chapter 1: Introduction & Pharmacopoeia 1. Define Pharmacopoeia. Write the main features of the Indian Pharmacopoeia (IP) . [Repeat: Very High] This is a foundational concept and a very frequent exam question. 2. Briefly describe the history of pharmacy education and profession in India. Understand the historical context of the pharmacy profession in India. Chapter 2: Packaging Materials 3. Compare glass and plastic as packaging materials, including their advantages, disadvantages, and how to choose between them. [Diagram] Expect a diagram-based question here . This topic is essential for understanding drug formulation. Chapter 3: Pharmaceutical Aids 4. Define preservatives. Classify them with examples and explain the uses of any four preservatives in pharmaceutical formulations. This is essential for ensuring drug formulation stability and safety. Chapter 4: Unit Operations [Most Important Chapter] 5. Explain the construction, working, and applications of a Ball Mill with a neat, labeled diagram. [Diagram] [Expected: 100%] This is a core unit operation and almost always appears in exams . 6. Describe the principle and working of a Fluidized Bed Dryer with a diagram. Why is freeze drying preferred for heat-sensitive drugs? Understand this key drying method and its comparative advantages. 7. What is size separation? Explain the working of a Cyclone Separator with a diagram. [Diagram] This is an important size separation technique. 8. Differentiate between mixing and blending. Explain the working of a Double Cone Blender with a diagram. [Diagram] This covers fundamental mixing equipment. Chapter 5: Solid Dosage Forms 9. Define tablets. Classify coated tablets with examples. Write the quality control tests for tablets. [High Yield] This is a core solid dosage form and a high-scoring topic for exams. 10. What are modified release tablets? Explain sustained-release and fast-dissolving tablets with examples. Understand this modern dosage form concept. 11. Describe the formulation and evaluation of Hard Gelatin Capsules . Why is controlling moisture so important? This is another major solid dosage form with practical relevance. Chapter 6: Liquid & Semi-Solid Dosage Forms 12. Define emulsion. Classify with examples. Describe the test to identify the type of emulsion . [Practical] This topic combines practical knowledge with theory and is common for liquid formulations. 13. Differentiate between ointments, creams, and gels, including their formulation bases and uses. These are key semi-solid dosage forms. 14. Write a note on suspensions : their types, ideal properties, and how to formulate Calamine Lotion. This is an important liquid dosage form with a practical example. Chapter 7: Sterile & Novel Formulations 15. What are parenterals? Write the essential quality control tests for injectable preparations . This covers critical sterile dosage forms. 16. Define novel drug delivery systems (NDDS). Classify them with two examples and list the advantages of any one system. This topic covers an emerging field in pharmaceutics. Chapter 8: Quality Assurance & GMP 17. Differentiate between Quality Control (QC) and Quality Assurance (QA). What is cGMP and why is it mandatory? These are foundational concepts for pharmaceutical manufacturing. Chapter-wise Bonus [High-Probability Short Notes] 18. Write short notes on: (a) Sieve standards as per IP (b) Triple roller mill (c) Membrane filtration These are important topics for short answer questions. 19. Explain the formulation steps of Paracetamol tablets with a flow chart. [Practical] This question links to practical work and a common formulation. 20. What is validation in pharmaceutical manufacturing? Why is calibration of equipment essential? These are key aspects of quality systems. SUBJECT 2: PHARMACEUTICAL CHEMISTRY (ER20-12T) Chapter 1: Impurities & Limit Tests [Most Repeated] 1. Explain the principle and procedure of the limit test for chlorides with chemical reactions. [Guaranteed Question] This is a guaranteed question and a fundamental analytical technique. 2. Describe the limit test for heavy metals using the thioacetamide method. Why is lead acetate paper used in the arsenic limit test? This is essential for controlling impurities. Chapter 2: Vo
