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- Generic Drugs: Questions Answers | FDA - U. S. Food and Drug . . .
Any generic medicine must perform the same in the body as the brand-name medicine It must be the same as a brand-name medicine in dosage, form and route of administration, safety, effectiveness
- Generic Drug Facts | FDA
A generic medicine is required to be the same as a brand-name medicine in dosage, safety, effectiveness, strength, stability, and quality, as well as in the way it is taken Generic medicines also
- U. S. Food and Drug Administration
Learn how to identify and avoid dangerous online pharmacies with FDA's BeSafeRx site and tips for buying medicines online safely
- Internet Pharmacy Warning Letters - FDA
Rogue online pharmacies offer potentially dangerous prescription drugs to U S consumers FDA has issued warning letters informing the website operators that they are engaged in illegal activity
- Generic Competition and Drug Prices | FDA - U. S. Food and Drug . . .
Estimated Savings from Generic Drug Approvals Estimating Cost Savings from New Generic Drug Approvals in 2021 (PDF, 692 KB) This study estimates savings from the 633 generic drug applications
- FDA List of Authorized Generic Drugs | FDA - U. S. Food and Drug . . .
An authorized generic is used to describe an approved brand name drug that is marketed as a generic product without the brand-name, or trade name, on the label It is the ex
- Frequently Asked Questions about Labeling for Prescription Medicines
Brand name, generic name or proper name, dosage form(s), route(s) of administration, and chemistry characteristics of the medicine (e g , chemical and structural formula, a list of active and
- Office of Generic Drugs 2023 Annual Report - FDA
In 2023 generic drugs continued to play a critical role in the U S health care system allowing patients greater access to needed medicines Generic drugs are generally lower cost than their brand
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