Generic drugs are mainly known as a drug sold or prescribed under the nonproprietary name of its active ingredients or under a generally descriptive name rather than under a brand or trade name. All inactive ingredients used in generic drugs are previously approved by the FDA. So two-third of prescriptions is filled with generic drugs. The reason is very simple. Doctors recommend Generic drugs as they provide the same medicines as the brands with the same results, but their prices are much more affordable for patients. The FDA also has high-quality and product-specific standards that must be adhered to for each batch of product as well as rigorous standards
Generic drugs manufactured, are required to assure the safety of their products. Based on comparisons, the FDA can determine if the brand and generic products are equivalent.
A generic medicine has to meet the same high standards as its brand counterpart to receive approval from the Food and Drug Administration (FDA). This means that the FDA must ensure that the generic and the brand have the same amount of active ingredients at the same strength, as well as the same dosage form, labeling and use. Generics must also follow the same high-quality manufacturing standards as the brand equivalents.
The Generic drugs like |
