Last updated on November 25th, 2024 at 04:01 pm
Generic medicines are manufactured by a variety of companies in different countries around the world. Many generic medicines are produced in countries with large and well-established pharmaceutical industries, such as India, China, and various countries in Europe.
In order to be approved for sale, a generic medicine must meet the same standards of safety, efficacy, and quality as its brand-name counterpart. This includes demonstrating that the generic medicine is the same as the brand-name medicine in terms of its active ingredient, dosage form, strength, intended use, and the conditions it is used to treat.
Food and Drug Administration (FDA) is responsible for regulating the manufacturing and distribution of generic medicines to ensure that they meet appropriate standards. The FDA has systems in place to ensure that generic medicines are manufactured in facilities that meet specific quality standards and that the medicines themselves meet the required standards of safety, efficacy, and quality.
Overall, generic medicines are manufactured in a variety of locations around the world and are subject to rigorous regulatory oversight to ensure their safety, efficacy, and quality.
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