B.PharmSemester 52025-26Industrial Pharmacy IBP502T

Industrial Pharmacy I (BP502T) - AKTU Question Paper 2025-26

B.Pharm · Semester 5 · Free PDF Download

This is the official AKTU Industrial Pharmacy I Previous Year Question Paper for B.Pharm Semester 5, academic session 2025-26. Published by Dr. A.P.J. Abdul Kalam Technical University (AKTU/UPTU), Lucknow. Free PDF download — no login required.

Course:B.Pharm
Semester:Semester 5
Session:2025-26
University:AKTU / UPTU

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Questions Asked in 2025-26

Industrial Pharmacy I (BP502T) — extracted question text · 75 marks · 3 Hours

Section AAttempt any two parts of thegollowing:
  • a
    Distinguish drugs on the basis of BCS classification
  • b
    What is the difference between amorphous and crystalline drugs in terms of stability?
  • c
    What is the role of binders in manufacturing tablets?
  • d
    Write in brief about IPQC test for capsule
  • e
    Differentiate between hard and soft gelatin capsules
  • f
    What are different sources of pyrogen contamination?
  • g
    Classify all types of glass used in pharmaceutical packaging
  • h
    ‘Explain significance of isotonicity in ophthalmic pr fis nitons. i, State the composition parameters of ions i j. Classify propellants used in aerosols. —_ < <q; * BCTION B
  • a
    Described various parameters ‘ef fhe in-process and finished product ae “eontrol tests for: coated tablets
  • b
    Describe various materials used for packaging of era with regards to their benefits, limitations and remedy to overcome such limitations
  • c
    Classify different types of parenteral products. How afte products evaluated for quality control? o-” : SECTION ey 3 Attempt any five parts of the following: & 7x5=35 « Amorphous or crystalline drug which will givyp wore stable dosage form and why? & Explain formulation considerations a and emulsions
  • c
    How will you formulate tooth pastbye explain and give preparation method for the same. & Discuss the in-process and finished product quality control tests for pharmaceutical aerosols based on pharmacopeia standards and specifications. @ Described the parameters of in-process and final product quality control tests for capsules
  • f
    How are dry powders for injection prepared by lyophilization?
  • g
    Discuss the evaluation of ophthalmic preparation as per pharmacopoeia standards and specifications

Question text is extracted from the official AKTU question paper PDF above. Check the original PDF for equations, diagrams and complete wording. Extracted: 2026-08-23.

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