Are there any restrictions or limitations on the use of generic drugs?

Yes, there are restrictions and limitations on the use of generic drugs in California. Generic drugs are drugs that are identical to brand-name drugs, but they are sold at a lower cost. In California, generic drugs must be approved by the U.S. Food and Drug Administration (FDA) to ensure the drug is safe and effective. It must also meet the same standards as the brand-name drug. The FDA requires generic drugs to be bioequivalent to the brand-name drug, meaning the drug must have the same active ingredient, strength, dosage form, and route of administration as the brand-name drug. Generic drugs must also be prescribed by a licensed doctor. The doctor must write the prescription for a generic drug if one is available. Pharmaceutical companies must also provide evidence of a generic drug’s effectiveness and safety to the FDA before it is approved for use. In addition, generic drugs must have the same packaging and labeling, including the expiration date and instructions for use, as the brand-name drug. Lastly, the FDA requires pharmacies to inform patients when they dispense a generic drug that is not equivalent to the brand-name drug.

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Are there any restrictions or limitations on the use of generic drugs?

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