Tag: Tablet uniformity

Types of Tablet Presses Used in Manufacturing Tablet presses are essential machines used in pharmaceutical manufacturing to compress powder blends into solid tablets of various shapes and sizes. There are several types of tablet presses available, each offering specific advantages and capabilities. Here are the different types of tablet presses commonly used in tablet manufacturing:…

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Manufacturing Orally Disintegrating Tablets (ODTs) Orally disintegrating tablets (ODTs), also known as fast-dissolving or quick-dissolving tablets, are a popular dosage form designed to rapidly disintegrate and dissolve in the mouth without the need for water. ODTs offer advantages in patient convenience and compliance, especially for individuals who have difficulty swallowing traditional tablets or capsules. The…

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Factors Affecting Tablet Dissolution Rate The dissolution rate of a tablet refers to how quickly the tablet disintegrates and releases the active pharmaceutical ingredient (API) into the surrounding medium, typically water, in a laboratory test. The dissolution rate is a critical parameter as it directly impacts the drug’s bioavailability and effectiveness. Several factors can influence…

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Tablet Weight Variation and Acceptable Limits Tablet weight variation is a critical quality parameter in tablet manufacturing that measures the consistency of tablet weight among a batch of tablets. It ensures that each tablet contains the correct amount of active pharmaceutical ingredient (API) and excipients, and that the tablets deliver the intended dose to patients….

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Comparison between Effervescent Tablets and Conventional Tablets 1. Composition and Formulation: Effervescent Tablets: Effervescent tablets contain active pharmaceutical ingredients (APIs) along with effervescent agents, such as citric acid and sodium bicarbonate. These agents react with water to produce carbon dioxide gas, leading to the characteristic effervescence or fizzing. Effervescent tablets often contain additional excipients like…

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Chewable Tablets: Formulation and Overview Introduction to Chewable Tablets Chewable tablets are a type of oral solid dosage form designed to be chewed or masticated before swallowing. They are formulated to provide a convenient and palatable way of administering medication, especially for patients who have difficulty swallowing conventional tablets or capsules. Chewable tablets are commonly…

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Measurement of Tablet Hardness Using Different Techniques Tablet hardness, also known as tablet crushing strength, is an essential parameter that measures the mechanical strength and integrity of a tablet. It is an important quality control parameter in tablet manufacturing. Several techniques are available to measure tablet hardness. Here are some commonly used methods: 1. Manual…

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Role of Binders in Tablet Formulation Binders are essential excipients used in tablet formulation to impart cohesiveness to the powders in the tablet blend. They play a crucial role in ensuring that the tablet maintains its shape and integrity during and after compression. Binders are necessary because many active pharmaceutical ingredients (APIs) and other excipients…

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Production of Effervescent Tablets and Their Advantages Production of Effervescent Tablets Effervescent tablets are a unique dosage form that rapidly dissolves in water, producing a pleasant effervescence (fizzing) due to the release of carbon dioxide. The production of effervescent tablets involves specific formulation and manufacturing techniques. Here’s an overview of the production process: Formulation The…

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Challenges in Manufacturing Sublingual Tablets Sublingual tablets are a specialized type of oral dosage form that is designed to be placed under the tongue, where the drug is rapidly absorbed into the bloodstream through the sublingual mucosa. While sublingual tablets offer several advantages, such as faster onset of action and avoidance of first-pass metabolism, their…

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Ensuring Content Uniformity in Tablet Production Content uniformity is a critical quality parameter in tablet production, ensuring that each tablet within a batch contains the correct and uniform amount of active pharmaceutical ingredient (API). Deviations in content uniformity can lead to dosing inaccuracies and affect the safety and efficacy of the medication. Here are the…

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