FDA Information

Metropolol has been approved by the U.S. Food and Drug Administration (FDA).

Mylan Laboratories, Inc., announced that the FDA has granted final approval for Mylan Pharmaceuticals' abbreviated new drug application, which provides for a new strength (25 mg) of metoprolol tartrate (a beta blocker).

President and COO Louis J. DeBone stated, "Mylan is the single largest generic supplier of metoprolol tartrate, in 50-mg and 100-mg strengths, in the United States. The addition of a new 25-mg strength further enhances our generic product portfolio and offers a convenient dosage alternative for patients and healthcare providers."

Please visit the official site of the FDA for further information.

 

FDA Information regarding Metoprolol

Why is this medication prescribed?

Other uses for this medicine

Dosage and using this medicine

What special precautions should I follow?

What should I do if I forget a dose?

What side effects can this medication cause?

What storage conditions are needed for this medicine?

In case of an emergency/overdose

 

This site is intended solely for U.S. audiences; products described here may be subject to different medical and/or regulatory requirements in other countries. This site is for educational purposes only; information contained within should not be used to diagnose or treat a health problem or disease. Please consult a licensed health care provider regarding your medical condition.The products mentioned are trademarks of their respective owners.