FAQ’s

Yes, generic medicines are rigorously tested and approved by regulatory authorities to ensure they meet the same safety and efficacy standards as branded drugs. They are considered safe and can be used with confidence.

The primary difference lies in the name, price, and appearance. Generic medicines are usually less expensive because they don’t require extensive research and marketing costs, while their quality, safety, and effectiveness are equivalent to their branded counterparts.

Generic manufacturers can produce medicines at a lower cost since they don’t have to invest in research, clinical trials, and marketing. This cost-saving is then passed on to consumers, making generic medicines more affordable.

Yes, most generic medicines require a prescription, just like branded drugs. It’s essential to consult with a qualified healthcare professional before starting any new medication to ensure it is suitable for your specific health condition.

In most cases, yes. Generic medicines are required to demonstrate bioequivalence to their branded counterparts, meaning they produce similar therapeutic effects. However, always consult your healthcare provider before making any changes to your medications

Generic medicines are sourced from reputable pharmaceutical manufacturers around the world, ensuring they meet strict quality standards and regulatory requirements.

Regulatory agencies closely monitor generic medicines’ production and distribution to ensure compliance with safety and quality standards. Look for approved and accredited sources when purchasing generic medications.

Yes, generic medicines undergo thorough testing to demonstrate their bioequivalence to branded drugs. Their effectiveness is comparable, providing the same therapeutic benefits.