Effervescent Tablets: Comprehensive Review on Formulation Strategies, Manufacturing Technologies, and Quality Evaluation


Authors : Dr. Arishasri Sundaramoorthy; Vignesh Rajappan; Renuga Durisamy; Rammohan Ravi; Vasantharaman Chandramohan; Bharathi Balakrishnan; Thirupathi sekar; Ananth kathalingam

Volume/Issue : Volume 10 - 2025, Issue 12 - December


Google Scholar : https://tinyurl.com/3b47k34x

Scribd : https://tinyurl.com/57ame72s

DOI : https://doi.org/10.38124/ijisrt/25dec989

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Abstract : Effervescent tablets are specialized oral dosage forms that have gained significant popularity in both pharmaceutical preparations and dietary supplement formulations due to their rapid disintegration and enhanced patient acceptability. These tablets contain a combination of acidic components such as citric or tartaric acid and alkaline components like sodium bicarbonate, which react in the presence of water to release carbon dioxide. The liberation of CO2 improves the solubility and palatability of the formulation, resulting in a clear, flavoured solution that is easy to administer, particularly for geriatric, paediatric, and dysphagic patients who have difficulty swallowing conventional tablets. Despite the advantages, effervescent tablets require careful selection and balance of excipients including binders, fillers, sweeteners, polymers, and water-soluble lubricants to maintain stability and prevent premature effervescent reactions. They are highly sensitive to moisture; therefore, manufacturing must be carried out under controlled environmental conditions, typically below 25°C and low humidity, with moisture-protective packaging to ensure product integrity. Various manufacturing methods such as wet granulation, dry granulation, direct compression, and advanced granulation technologies are utilized to produce tablets with suitable mechanical strength and dissolution properties. Quality evaluation parameters including hardness, friability, effervescence time, pH, moisture content, and uniformity of content are essential for ensuring therapeutic performance. Although effervescent tablets provide rapid onset of action, improved taste, and patient compliance, challenges such as higher production cost and specialized equipment requirements remain. Continued advancements in formulation and process technologies are supporting the growing application and commercial importance of effervescent tablet systems.

Keywords : Effervescent Tablets; Acid–Base Reaction; Bioavailability; Manufacturing Techniques; Patient Compliance.

References :

  1. F. Naseem, S. U. Shah, S. A. Rashid, A. Farid, M. Almehmadi and S. Alghamdi, Metronidazole Based Floating Bioadhesive Drug Delivery System for Potential Eradication of H. pylori: Preparation and In Vitro Characterization, Polymers, 2022, 14(3), 519, DOI: 10.3390/ polym14030519.
  2. Machmud E. Effectiveness of Roselle Effervescent Tablets as Traditional Medicinal Plants in preventing the Growth of Candida albicans Colonies and Streptococcus mutans. J Contemp Dent Pract. 2018 Aug;19(8):925–8.
  3. Machmud E. Effectiveness of Roselle Effervescent Tablets as Traditional Medicinal Plants in preventing the Growth of Candida albicans Colonies and Streptococcus mutans. J Contemp Dent Pract. 2018 Aug;19(8):925–8.
  4. Indian Pharmacopoeia Commission, Gh Viscosity. The Indian Pharmacopoeia Government. of India, Ministry of Health & Family Welfare, 2018; 252-253.
  5. Pham JH. Understanding effervescent tableting technology [cited 2015 Nov 29].
  6. Rani, M. S. Review on introduction to effervescent tablets and granules. Kenkyu Journal of Pharmacology, 2020; 6: 1-11.
  7. Biranje S, More A, Shangrapawar TP, Bhosale PDEA A. A Review on Formulation and Evaluation of Effervescent Tablets. Int J Pharm Pharm Res. 2021; 21(3):476-86.
  8. Juarez-Enriquez E, Olivas GI, Zamudio-Flores PB, Ortega-Rivas E, Perez-Vega S, Sepulveda DR. Effect of water content on the flowability of hygroscopic powders. J Food Eng. 2017 Jul 1; 205:127
  9. Apostolopoulos D, Fusi R. Prediction of moisture barrier requirements for an effervescent single-serve aspartame-sweetened tablet. Development in Food Science. 1995; 37:1119-32.
  10. methods37. Jagrati, K. M., & Sengar, A. Liposomal vesicular delivery system: An innovative nano carrier. World Journal of Pharmaceutical Research, 2024; 13(13): 1155-1169.
  11. Prajapati, R. N., Jagrati, K., Sengar, A., & Prajapati, S. K. Nanoparticles: Pioneering the future of drug delivery and beyond. World Journal of Pharmaceutical Research, 2024; 13(13): 1243-1262
  12. X. Dong, W. Zhang, X. Wang, S. Liu, J. Liang, C. Liufu, S. Zeng, J. Pang, S. Li, L. Xiong, G. Zhou, W. Zhu,    H. Lao, Z. Lin and F. Yang, A Novel Preparation Method for Effervescent Tablets of Xianganfang Containing Fresh Juice using a Semi-Solid Extrusion 3D Printer with Three Cartridge Holders, AAPS PharmSciTech, 2022, 23(6), 193, DOI: 10.1208/s12249-022-02336-3.
  13. Y. Wang, S. Xu, Z. Xiao, Y. Jiang, Q. Jiang, J. Li and W. He, Stiripentol Enteric Solid Dispersion-Loaded Effervescent Tablets: Enhanced Dissolution, Stability, and Absorption, AAPS PharmSciTech,2022, 23(5), 141, DOI: 10.1208/s12249 022-02261-5.
  14. M. Rosch, K. Lucas, J. Al-gousous, U. Pöschl and P. Langguth, Formulation and Characterization of an Effervescent Hydrogen–Generating Tablet, Pharmaceuticals 2021, 14(12), 1327, DOI: 10.3390/ph14121327.
  15. M. Israr, N. Pugliese, A. Farid, S. Ghazanfar, A. Di Cerbo, M. Muzammal, A. S. Alamri, S. M. B. Asdaq, A. Ahmad and K. A. Khan, Preparation and Characterization of Controlled-Release Floating Bilayer Tablets of Esomeprazole and Clarithromycin, Molecules, 2022, 27(10), 3242, DOI: 10.3390/molecules27103242.
  16. M. Rahamathulla, S. Saisivam, A. Alshetaili, U. Hani, H. V. Gangadharappa, S. Alshehri, M. M. Ghoneim and F. Shakeel, Design and evaluation of losartan potassium effervescent floating matrix tablets: In vivo X-ray imaging and pharmacokinetic studies in albino rabbits, Polymers, 2021, 13(20), 3476, DOI: 10.3390/polym13203476.
  17. P. Thapa and S. H. Jeong, Effects of formulation and process variables on gastroretentive floating tablets with a high-dose soluble drug and experimental design approach, Pharmaceutics, 2018, pharmaceutics10030161.
  18. S. S. Smail, N. J. Ibrahim and N. R. Hussein, Development and In Vitro Evaluation of Buccal Effervescent Tablet Containing Ropinirole Hydrochloride, Polytech. J., 2019, 9(2), 37–41, DOI: 10.25156/ptj.v9n2y2019
  19. S. Taymouri, A. Mostafavi and H. Mahmoodi, Formulation, Design, and Optimization of Taste-Masked Effervescent Tablet Containing Methocarbamol, Iran. J. Pharm. Sci., 2021, 2021(4), DOI: 10.22037/ijps.v17.40234.
  20. P. B. Savant, M. A. Qureshi, N. Kshirsagar, M. Kareppa, A. B. Thalkari, and P. N. Karwa, Preparation and Evaluation of Diclofenac Sodium Effervescent Tablet,  J. Pharm., 2021, 305–311, DOI: 10.52711/0975-4377.2021.00050
  21. foldvari M Nanopharmaceutics Innovations in Gene Therapy: Moving Towards Non-Viral and Non-Invasive Delivery Methods. J Nanomedine Biotherapeutic Discovery, 2014; 4: 135.
  22. Rajalakshmi G, Vamsi CH, Balachandar R, Damodharan N. Formulation and evaluation of diclofenac potassium effervescent tablets. Int J Pharm Biomed Res. 2011;2(4):237–43.
  23. Stahl H. Effervescent dosage manufacturing process. Pharm Technol Eur 2003;15:25–8.
  24. Eichman and Robinson Mechanistic studies on effervescent-induced permeability enhancement. Pharmaceutical Research, 1998; 15(6): 925-930.
  25. BG, P., & O, M. Concept, manufacturing, and characterization of effervescent tablets: A review. SunText Review of Pharmaceutical Sciences, 2021; 2(1).
  26. Stahl H. Effervescent dosage manufacturing process. Pharm Technol Eur 2003;15:25–8.
  27. Foldvari, M. Nanopharmaceutics innovations in gene therapy: Moving towards non-viral and non-invasive delivery methods. Journal of Nanomedicine & Biotherapeutic Discovery, 2014; 4(135).
  28. Simone V De, Caccavo D, Dalmoro A, Lamberti G, d'Amore M, Barba AA. Inside the Phenomenological Aspects of Wet Granulation: Role of Process Parameters. In: Granularity in Materials Science. InTech; 2018. p. 63-84.
  29. Zheng X, Wu F, Hong Y, Shen L, Lin X, Feng Y. Improvements in the sticking, hygroscopicity, and compactibility of effervescent systems by fluid-bed coating. RSC Adv. 2019; 9(54):31594-608
  30. p. Jean Bru. Process for manufacturing effervescent granules and tablets. Vol. 614. France: United states Patent; 4614648, 198301-7.
  31. Liu B, Wang J, Zeng J, Zhao L, Wang Y, Feng Y, et al. A review of high shear wet granulation for better process understanding, control and product development. Powder Technol. 2021 Mar 1; 381:204 23.
  32. Haack D, Gergely I, Metz C. The TOPO Granulation Technology Used in the Manufacture of Effervescent Tablets New, user friendly dosage forms enable product line extensions. TechnoPharm 2. 2012; Nr. 3:186-91.
  33. Lima AL, Pinho LAG, Chaker JA, Sa-Barreto LL, Marreto RN, Gratieri T, et al. Hot-melt extrusion as an advantageous technology to obtain effervescent drug products. Pharmaceutics. 2020 Aug 1; 12(8):1-20.
  34. Tawar M, Raut K, Chaudhary R, Jain N. Solubility Enhancement of Resveratrol by Effervescence Assisted Fusion Technique. Research Journal of Pharmaceutical Dosage Forms and Technology 2022; 14(4):293-8.
  35. Yanze FM, Duru C, Jacob M. A Process to Produce Effervescent Tablets: Fluidized Bed Dryer Melt Granulation. Drug Dev Ind Pharm [Internet]. 2000; 26(11):1167-76.
  36. Murray RB. New Approach to the Fusion Method for Preparing Granular Effervescent Products. Industrial Pharmaceutical technology. 1968; 57(10):1776-9.
  37. Yanze FM, Duru C, Jacob M, A process to produce effervescent tablets: Fluidized bed dryer melt granulation. Drug Development & Industrial Pharmacy, 2000; 26(11): 1167-76.
  38. Simona B, Tanja R, Using different experimental designs in drug excipient Compatibility Studies during the Pre- formulation development of a stable solid dosage formulation, Acta Chimica Slovenica, 2010; 57: 895-903.
  39. Larry LA and Stephan WH, Pharmaceutical Dosage Form: Tablets 3rd edition, 1: 465.
  40. Aboud HM, Elbary A, Ali AA, Enhanced dissolution of meloxicam from orodispersible tablets prepared by different methods, Bulletin of Faculty of Pharmacy, Cairo University, 2012; 50: 89–97.
  41. Ahmed I, Aboul-Einien M, In vitro and in vivo evaluation of a fast disintegrating lyophilized dry emulsion tablet containing griseofulvin, European Journal of Pharmaceutical Sciences, 2007; 32: 58–68.
  42. Dhakar RC, Maurya SD, Dangi G, Kumar G, Gupta M, Kirori Wal S, Buccal Adhesive Dosage Forms As A NISDD: A Pharmaceutical Review, Research Pharmaceutica, 2010; 1(1): 46-59.
  43. Aly AM, Amro BI, Hajji FD, Preparation and Evaluation of Rapidly Disintegrating Glimepiride Tablets. International Journal of Pharmaceutical Sciences and Nanotechnology, 2011; 3(4): 1220-1229.
  44. Ashish P, Harsoliya MS, Pathan JK, Shruti S, A Review- Formulation of Mouth Dissolving tablet, International Journal of Pharmaceutical and Clinical Science, 2011; 1(1): 1-8.
  45. Sandhyarani G, Kumar KP, Formulation and evaluation of fast dissolving Tablet of imidapril, Indian Journal of Pharmaceutical Science& Research, 2017; 4(3): 147-150.
  46. Dhakar RC, Maurya SD, Gupta AK, Siddiqui AW, Interpenetrating polymeric network hydrogel for stomach- specific drug delivery of clarithromycin: Preparation and evaluation, Asian Journal of Pharmaceutics, 2010; 4(4): 184-189
  47. S. G. Patel and M. Siddaiah, Formulation and evaluation of effervescent tablets: a review, J. Drug Delivery Ther., 2018, 8(6), 296–303, DOI: 10.22270/jddt.v8i6.2021
  48. Uniformity of Weight of Single-Dose Preparations . In: Indian Pharmacopoeia 2018. The Indian Pharmacopoeia Commission, Indian Pharmacopoeia Laboratory, Govt. of India, Ministry of Health & Family Welfare; 2018. p. 308.
  49. Lodhi VD, Jadon AS, Sen J, Jain PK, Thakur BS, Khare B, et al. Effervescent Tablets: Everything You Need To Know. Asian Journal of Dental and Health Sciences. 2022 Dec 15; 2(4):1-8. https://doi.org/10.22270/ajdhs.v2i4.18

Effervescent tablets are specialized oral dosage forms that have gained significant popularity in both pharmaceutical preparations and dietary supplement formulations due to their rapid disintegration and enhanced patient acceptability. These tablets contain a combination of acidic components such as citric or tartaric acid and alkaline components like sodium bicarbonate, which react in the presence of water to release carbon dioxide. The liberation of CO2 improves the solubility and palatability of the formulation, resulting in a clear, flavoured solution that is easy to administer, particularly for geriatric, paediatric, and dysphagic patients who have difficulty swallowing conventional tablets. Despite the advantages, effervescent tablets require careful selection and balance of excipients including binders, fillers, sweeteners, polymers, and water-soluble lubricants to maintain stability and prevent premature effervescent reactions. They are highly sensitive to moisture; therefore, manufacturing must be carried out under controlled environmental conditions, typically below 25°C and low humidity, with moisture-protective packaging to ensure product integrity. Various manufacturing methods such as wet granulation, dry granulation, direct compression, and advanced granulation technologies are utilized to produce tablets with suitable mechanical strength and dissolution properties. Quality evaluation parameters including hardness, friability, effervescence time, pH, moisture content, and uniformity of content are essential for ensuring therapeutic performance. Although effervescent tablets provide rapid onset of action, improved taste, and patient compliance, challenges such as higher production cost and specialized equipment requirements remain. Continued advancements in formulation and process technologies are supporting the growing application and commercial importance of effervescent tablet systems.

Keywords : Effervescent Tablets; Acid–Base Reaction; Bioavailability; Manufacturing Techniques; Patient Compliance.

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31 - January - 2026

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