FDA Information
Finasteride was approved initially by the US Food and Drug Administration (FDA) in 1992 as Proscar®, a treatment for prostate enlargement, but the sponsor - Merck & Co. - demonstrated in further clinical studied that using 1 mg of finasteride was effective in treating hair growth in male pattern hair loss. As a result, in December 22nd 1997, the FDA approved finasteride (Propecia®) to treat male pattern hair loss.
On June 19th 2006, Merck's patents on Proscar® and Propecia® expired and the FDA approved a first-time generic formulation for finasteride 5 mg tablets. As a result, Cipla is also manufacturing finasteride (under the brand names Fincar® and Finpecia®), as is Dr. Reddy's (Finax® and Finast®), Ranbaxy (Finara®), and Aleppo Pharmaceuticals (Prosteride®).
Please visit the official site of the FDA for further information.
Why is this medication prescribed?
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