How to Choose Between Generic and Brand Name Medication
Understand that generic and brand name drugs contain the same active ingredient., Know that generic and brand name drugs are identical in strength., Understand that generic and brand name drugs must meet the same quality standards., Realize that...
Step-by-Step Guide
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Step 1: Understand that generic and brand name drugs contain the same active ingredient.
The U.S.
Food and Drug Administration requires that generic drugs contain the same active ingredient as the respective brand name drug.
This means both generics and brand name medications contain the same active drug, which will have the same effect in your body., The FDA requires that brand name drugs and their generic equivalents are administered in the same manner, have the same dosage form, and are equivalent in strength., The FDA requires that generic drugs meet the exact same batch requirements for identity, strength, purity, and quality as their brand name counterparts.
Generics also must be manufactured under the same strict FDA manufacturing regulations that the industry requires for innovator products.These are requirements for all brands, generic or not, of a particular drug. , This means that the U.S.
Food and Drug Administration requires the drug manufacturer to demonstrate through clinical study that, after a patient takes a generic drug, the amount of the drug in the patient’s bloodstream is at the same level as when a patient takes the brand name drug.
If the levels are equivalent, the drug will work the same.The FDA requires this of all generic brands of the same drug. -
Step 2: Know that generic and brand name drugs are identical in strength.
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Step 3: Understand that generic and brand name drugs must meet the same quality standards.
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Step 4: Realize that generic drugs must perform the same as the brand name drug.
Detailed Guide
The U.S.
Food and Drug Administration requires that generic drugs contain the same active ingredient as the respective brand name drug.
This means both generics and brand name medications contain the same active drug, which will have the same effect in your body., The FDA requires that brand name drugs and their generic equivalents are administered in the same manner, have the same dosage form, and are equivalent in strength., The FDA requires that generic drugs meet the exact same batch requirements for identity, strength, purity, and quality as their brand name counterparts.
Generics also must be manufactured under the same strict FDA manufacturing regulations that the industry requires for innovator products.These are requirements for all brands, generic or not, of a particular drug. , This means that the U.S.
Food and Drug Administration requires the drug manufacturer to demonstrate through clinical study that, after a patient takes a generic drug, the amount of the drug in the patient’s bloodstream is at the same level as when a patient takes the brand name drug.
If the levels are equivalent, the drug will work the same.The FDA requires this of all generic brands of the same drug.
About the Author
Isabella Richardson
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