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Generic Medicine & Branded Medicine both are same
If a generic medicine and a branded medicine contain the same active ingredient, dosage form, strength, and route of administration, they are considered to be bioequivalent. This means that they are expected to have the same therapeutic effect in the body when taken in the same dose.
Regulatory authorities require generic medicines to demonstrate bioequivalence to the corresponding branded medicine through rigorous testing. This ensures that the generic medicine is absorbed and distributed in the body in a similar manner and to a similar extent as the branded medicine.
While generic and branded medicines are expected to be therapeutically equivalent, there may be slight variations in inactive ingredients (also known as excipients) between different formulations. These variations in excipients do not affect the therapeutic action of the active ingredient, but they may impact factors such as taste, appearance, or the potential for allergic reactions in some individuals.
It's important to note that generic medicines undergo the same rigorous testing and regulatory scrutiny as branded medicines to ensure their safety, efficacy, and quality. Generic medicines can be a cost-effective alternative to branded medicines as they are typically less expensive due to lower research and development costs, marketing expenses, and the presence of competition among manufacturers.
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