The terms nutraceuticals and nutraceutical supplements is an outgrowth of the combination of the terms “nutritional” and “pharmaceutical”. Supplement and vitamin suppliers and companies were looking for a better way to describe the products they manufactured that encompassed vitamins, minerals and nutritional health supplements. As a result, the phrases “nutraceuticals” and “nutraceutical supplements” have emerged. Therefore, nutraceutical companies manufacture and sell nutritional products such as vitamins, minerals and health supplements. There are currently a wide range of supplement manufacturing companies in the USA.
A generic drug is a chemically equivalent, lower-cost version of a brand-name drug, costing 30-80% less! A brand-name drug and its generic version must have the same active ingredient, dosage, safety, strength, usage directions, quality, performance and intended use.
Yes. Generic and brand-name drugs must meet the exact same standards for effectiveness, safety and quality.
Yes. The Food and Drug Administration (FDA) requires generic drugs to have the same quality, strength, purity and stability as their brand-name versions. Generic drugs are thoroughly tested to make sure their performance and ingredients meet the FDA’s standards for equivalency.
No. Both brand-name and generic drug facilities must meet the same standards; the FDA won’t permit drugs to be made in substandard facilities. The FDA conducts about 3,500 inspections a year to ensure standards are met. In fact, brand-name firms are linked to an estimated 50% of generic drug production. They frequently make generic copies of their own or other brand-name drugs, then sell them with a generic name.