Tag: bioequivalence
Dissolution Testing: How the FDA Ensures Generic Drug Quality
Dissolution testing is how the FDA ensures generic drugs release their active ingredients at the same rate as brand-name versions, proving bioequivalence without human trials. It's a precise, science-backed process that keeps generics safe and affordable.
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Bioequivalence for Inhalers, Patches, and Injections: How Generic Drugs Match the Real Thing
Bioequivalence for inhalers, patches, and injections isn't just about matching drug amounts-it's about ensuring the drug reaches the right place in your body the same way as the brand. Here's how regulators make sure generics work.
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Generic vs Brand Name Drugs: What the Label Really Tells You
Generic drugs are just as effective as brand-name versions, but cost up to 90% less. Learn how the FDA ensures therapeutic equivalence, what label differences really mean, and when to choose generics safely.
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