Are there any restrictions or limitations on the substitution of generic drugs for brand name drugs?

In Pennsylvania, generic drugs can be substituted for brand name drugs as long as certain restrictions and limitations are met. A generic drug must be approved by the Food and Drug Administration (FDA) and meet the same standards of quality, safety and effectiveness as the brand name drug. Additionally, a generic drug must have the same active ingredient, strength, dosage form, and route of administration as the brand name drug. In most cases, a generic drug can only be prescribed if the brand name drug is not available or if it is more cost effective for the patient. Pharmacists must receive permission from the prescribing physician to substitute a generic substitute for a brand name drug. If the pharmacy does not obtain permission, then the prescription must be filled according to the prescribing physician’s directions. In addition, the pharmacist must provide the patient with a written notification that a generic drug is being substituted. The notification must include the name and strength of the generic drug and a statement that the generic drug is therapeutically equivalent to the brand name drug. It is important to note that some medications cannot be substituted with a generic drug, such as controlled substances and certain combination products. It is best to consult with your doctor or pharmacist to determine if a generic substitute is available for your medication.

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Are there any restrictions or limitations on the substitution of generic drugs for brand name drugs?

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