Same FDA Requirements - BlueAdvantage Administrators of Arkansas

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Same FDA Requirements

Same FDA Requirements
	Brand-Name Drug	Generic Drug
For reformulations of a brand-name drug or generic versions of a drug, the FDA reviews data showing the drug is bioequivalent to the one used in the original safety and efficacy testing.
FDA evaluates the manufacturer's adherence to good manufacturing practices before the drug is marketed.
FDA reviews the active and inactive ingredients used in the formulation before the drug is marketed.
FDA reviews the actual drug product.
FDA reviews the drug's labeling.
Manufacturer must seek FDA approval before making major manufacturing changes or reformulating the drug.
Manufacturer must report adverse reactions and serious adverse health effects to the FDA.
FDA periodically inspects manufacturing plants.
FDA monitors drug quality after approval.

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