Find Information about a Drug | FDA
2022年8月9日 · Find Drug Information on MedlinePlus. Easy-to-use resource from NIH with information about side effects, dosage, special precautions, and more for prescription and …
Where and How to Dispose of Unused Medicines | FDA - U.S. Food …
2024年4月2日 · The best way to dispose of your expired, unwanted, or unused medicines is through a drug take back program. Or you can do it at home. ... (OTC) drugs in pills, liquids, …
FDA Approves Novel Non-Opioid Treatment for Moderate to …
2025年1月30日 · Today, the U.S. Food and Drug Administration approved Journavx (suzetrigine) 50 milligram oral tablets, a first-in-class non-opioid analgesic, to treat moderate to severe …
Drug Quality Sampling and Testing Programs | FDA - U.S. Food …
To help ensure that high-quality drugs are sold in the U.S., CDER maintains a comprehensive quality surveillance program. A critical function of this program is testing selected drugs in FDA ...
FDA Approves First Medication for Obstructive Sleep Apnea
Español. Today, the U.S. Food and Drug Administration approved Zepbound (tirzepatide) for the treatment of moderate to severe obstructive sleep apnea (OSA) in adults with obesity, to be …
Drug Disposal: Drug Take-Back Options | FDA - U.S. Food and …
2024年10月31日 · These drug take-back locations safely and securely gather and dispose of your unused or expired medicines, including those that contain controlled substances. In your …
Questions and Answers on Mifepristone for Medical Termination …
Mifepristone is a drug that blocks a hormone called progesterone that is needed for a pregnancy to continue. ... New York Woman Sentenced for Selling Abortion-Inducing Pills Illegally …
Counterfeit Medicine | FDA - U.S. Food and Drug Administration
The U.S. drug supply is among the safest in the world. The U.S. has federal and state laws that create a “closed” drug distribution system to help ensure the U.S. drug supply is safe.
Compounding and the FDA: Questions and Answers | FDA - U.S.
2024年11月15日 · A generic drug is approved by FDA under 505(j) of the FD&C Act and meets all of the requirements of that section (including establishing therapeutic equivalence to a brand …
Drugs | FDA - U.S. Food and Drug Administration
The Center for Drug Evaluation and Research (CDER) ensures that safe and effective drugs are available to improve the health of the people in the United States