Who is responsible for regulating Suhagra 25 Mg ?

Suhagra 25 mg (which contains Sildenafil) falls under the responsibility of national and international health authorities, such as: The Food and Drug Administration (FDA) – In the United States, the FDA is responsible for approving and regulating all prescription medications, including Suhagra. They ensure that the medication is safe, effective, and correctly labeled. The European Medicines Agency (EMA) – In Europe, the EMA oversees the regulation of pharmaceuticals, ensuring they meet safety and efficacy standards. National Drug Regulatory Authorities – In other countries, such as India (where Suhagra 25 Mg is commonly produced), the Drugs Controller General of India (DCGI) regulates and approves medicines. These organizations ensure that Suhagra 25 mg and other medications on the market meet the required safety standards and are prescribed correctly to minimize risks.