Generic Name

Finasteride

Brand Names
Propecia, Proscar
FDA approval date: December 15, 2006
Classification: 5-alpha Reductase Inhibitor
Form: Tablet

What is Propecia (Finasteride)?

For many men, hair loss can be more than a cosmetic concern, it can affect self-esteem, confidence, and overall emotional well-being. Propecia (finasteride) offers an effective medical option for men experiencing male pattern hair loss, helping them regain not just hair, but also confidence in their appearance. 

Propecia is a prescription medication used to treat androgenetic alopecia (male pattern baldness) in adult men. It belongs to a class of drugs known as 5-alpha-reductase inhibitors, which influence hormone levels related to hair growth. Unlike topical treatments, Propecia works from within the body to slow hair loss and, in many cases, promote regrowth. Approved by the U.S. Food and Drug Administration (FDA) in 1997, Propecia remains one of the most studied and widely prescribed oral medications for male hair loss today. 

What does Propecia do? 

Propecia is prescribed to treat male pattern hair loss, a common condition caused by a combination of genetics and hormonal changes. Over time, hair follicles in certain areas of the scalp shrink and produce thinner, shorter hairs eventually leading to visible baldness, especially on the crown and hairline. 

Propecia works to slow down or stop further hair loss and can stimulate regrowth in some men. Clinical studies have shown that continuous use of finasteride leads to improved hair density and prevents further loss in up to 90% of men who take it for at least one year (NIH, 2024). The benefits are usually seen after several months of consistent treatment, and continued use is necessary to maintain results. 

While Propecia does not cure baldness or restore hair in completely bald areas, it can significantly delay progression and help men preserve their existing hair longer, improving appearance and confidence. 

How does Propecia work? 

Propecia contains finasteride, which works by targeting the root hormonal cause of male pattern baldness. In men, testosterone is naturally converted into a more potent hormone called dihydrotestosterone (DHT) by an enzyme known as 5-alpha-reductase. 

In genetically susceptible men, DHT causes hair follicles particularly those at the front and crown of the scalp to shrink over time. This process, known as miniaturization, results in thinner hair strands and shorter growth cycles until follicles stop producing hair altogether. 

Propecia blocks the action of the 5-alpha-reductase enzyme, reducing DHT levels in the scalp by up to 60–70%. Lower DHT levels help protect hair follicles from shrinking, allowing them to continue producing healthy, thicker hair. 

Clinically, this mechanism is significant because it addresses the underlying hormonal driver of male pattern hair loss, rather than just treating surface symptoms. This makes Propecia one of the few therapies proven to both prevent further hair loss and promote regrowth in men. 

Propecia side effects 

Most men tolerate Propecia well, but as with all medications, side effects can occur. Understanding them helps patients make informed decisions and feel reassured during treatment. 

Common side effects may include: 

  • Decreased sex drive (libido) 
     
  • Difficulty achieving or maintaining an erection 
     
  • Reduced semen volume 

These effects are typically mild and reversible after stopping the medication or with continued use as the body adjusts. Only a small percentage of men (around 2–4%) experience these symptoms (FDA, 2023). 

Serious but rare side effects include: 

  • Persistent sexual side effects after discontinuation (post-finasteride syndrome — very uncommon and still under study) 
     
  • Breast tenderness, enlargement, or lumps 
     
  • Testicular pain 
     
  • Signs of allergic reaction such as rash, itching, or swelling 

Men should seek medical attention if they experience breast changes, swelling of lips or face, or depression or anxiety while on the medication. 

Who should avoid Propecia: 

  • Women and children should not take or handle crushed or broken tablets, as exposure can cause birth defects in unborn male babies. 
     
  • Men with known allergies to finasteride or similar drugs should not use it. 

Doctors may periodically review a patient’s overall health, monitor hormone-related symptoms, and evaluate treatment response to ensure safe and effective long-term use. 

Propecia dosage 

Take Propecia once daily, by mouth, with or without food. Consistent daily use for 3-6 months shows visible improvement. Benefits reverse within 12 months if discontinued. 

Doctors may advise follow-ups to track treatment and side effects. While no routine blood tests are needed, some clinicians may check PSA levels as finasteride can lower them. 

Older adults can generally use Propecia safely, though it is not typically prescribed for men over 65 because male pattern baldness progression usually stabilizes naturally at that age. 

Does Propecia have a generic version? 

Yes. Finasteride is the generic version of Propecia, and it is FDA-approved. Generic finasteride tablets contain the same active ingredient, dosage strength, and therapeutic effect as brand-name Propecia. The main difference lies in appearance, inactive ingredients, and cost. 

Generic finasteride offers an affordable, effective, and safe alternative to Propecia for hair loss. Finasteride is also sold as Proscar, a higher-strength version for enlarged prostate (BPH); patients should confirm they receive the correct formulation for hair loss. 

Conclusion 

Propecia (finasteride) is a trusted, scientifically proven treatment for male pattern baldness that helps men preserve their hair and confidence over time. By blocking the hormone responsible for follicle shrinkage, it slows hair loss and promotes visible regrowth in many users. 

Propecia is generally safe and effective for male hair loss when prescribed and monitored by a doctor. Consistent use is crucial for gradual, long-term results. Always consult your doctor before starting or stopping treatment and maintain open communication. 

References 

  1. U.S. Food and Drug Administration (FDA). (2023). Propecia (finasteride) prescribing information. Retrieved from https://www.accessdata.fda.gov 
     
  1. Mayo Clinic. (2024). Finasteride (oral route) drug information. Retrieved from https://www.mayoclinic.org 
     
  1. MedlinePlus. (2024). Finasteride: Uses, side effects, and precautions. National Library of Medicine. Retrieved from https://medlineplus.gov 
     
  1. National Institutes of Health (NIH). (2024). Finasteride and androgenetic alopecia clinical studies. Retrieved from https://www.nih.gov 
     

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Brand Information

    PROPECIA (finasteride)
    1INDICATIONS AND USAGE
    PROPECIA
    Efficacy in bitemporal recession has not been established.
    PROPECIA is not indicated for use in women.
    2DOSAGE AND ADMINISTRATION
    PROPECIA may be administered with or without meals.
    The recommended dose of PROPECIA is one tablet (1 mg) taken once daily.
    In general, daily use for three months or more is necessary before benefit is observed. Continued use is recommended to sustain benefit, which should be re-evaluated periodically. Withdrawal of treatment leads to reversal of effect within 12 months.
    3DOSAGE FORMS AND STRENGTHS
    PROPECIA tablets (1 mg) are tan, octagonal, film-coated convex tablets with "stylized P" logo on one side and PROPECIA on the other.
    4CONTRAINDICATIONS
    PROPECIA is contraindicated in the following:
    • Pregnancy. Finasteride use is contraindicated in women when they are or may potentially be pregnant. Because of the ability of Type II 5α-reductase inhibitors to inhibit the conversion of testosterone to 5α-dihydrotestosterone (DHT), finasteride may cause abnormalities of the external genitalia of a male fetus of a pregnant woman who receives finasteride. If this drug is used during pregnancy, or if pregnancy occurs while taking this drug, the pregnant woman should be apprised of the potential hazard to the male fetus.
    • Hypersensitivity to any component of this medication.
    5OVERDOSAGE
    In clinical studies, single doses of finasteride up to 400 mg and multiple doses of finasteride up to 80 mg/day for three months did not result in adverse reactions. Until further experience is obtained, no specific treatment for an overdose with finasteride can be recommended.
    Significant lethality was observed in male and female mice at single oral doses of 1500 mg/m
    6DESCRIPTION
    PROPECIA (finasteride) tablets contain finasteride as the active ingredient. Finasteride, a synthetic 4-azasteroid compound, is a specific inhibitor of steroid Type II 5α-reductase, an intracellular enzyme that converts the androgen testosterone into 5α-dihydrotestosterone (DHT).
    The chemical name of finasteride is
    image of finasteride chemical structure
    Finasteride is a white crystalline powder with a melting point near 250°C. It is freely soluble in chloroform and in lower alcohol solvents but is practically insoluble in water.
    PROPECIA (finasteride) tablets are film-coated tablets for oral administration. Each tablet contains 1 mg of finasteride and the following inactive ingredients: lactose monohydrate, microcrystalline cellulose, pregelatinized starch, sodium starch glycolate, hydroxypropyl methylcellulose, hydroxypropyl cellulose, titanium dioxide, magnesium stearate, talc, docusate sodium, yellow ferric oxide, and red ferric oxide.
    7HOW SUPPLIED/STORAGE AND HANDLING
    PROPECIA tablets, 1 mg, are tan, octagonal, film-coated convex tablets with "stylized P" logo on one side and PROPECIA on the other. They are supplied as follows:
    • NDC 78206-152-01 bottles of 30 (with desiccant)
    • NDC 78206-152-02 PROPAK® bottles of 90 (with desiccant).
    8PATIENT COUNSELING INFORMATION
    Advise the patient to read the
    Exposure of Women — Risk to Male Fetus
    Physicians should inform patients that women who are pregnant or may potentially be pregnant should not handle crushed or broken PROPECIA tablets because of the possibility of absorption of finasteride and the subsequent potential risk to a male fetus. PROPECIA tablets are coated and will prevent contact with the active ingredient during normal handling, provided that the tablets have not been broken or crushed. If a woman who is pregnant or may potentially be pregnant comes in contact with crushed or broken PROPECIA tablets, the contact area should be washed immediately with soap and water
    Increased Risk of High-Grade Prostate Cancer
    Patients should be informed that there was an increase in high-grade prostate cancer in men treated with 5α-reductase inhibitors indicated for BPH treatment, compared to those treated with placebo in studies looking at the use of these drugs to prevent prostate cancer
    Sexual Adverse events
    Physicians should inform the patients that PROPECIA may cause symptoms of sexual dysfunction such as decreased libido, erectile dysfunction, and ejaculation disorder, including decreased ejaculate volume.
    Additional Instructions
    Physicians should instruct their patients to promptly report any changes in their breasts such as lumps, pain or nipple discharge. Breast changes including breast enlargement, tenderness and neoplasm have been reported
    Physicians should instruct their patients to read the patient package insert before starting therapy with PROPECIA and to read it again each time the prescription is renewed so that they are aware of current information for patients regarding PROPECIA.
    9PRINCIPAL DISPLAY PANEL - 1 mg Tablet Bottle Label
    NDC 78206-152-01
    Propecia
    Each tablet contains 1 mg finasteride.
    Rx only
    30 Tablets
    PRINCIPAL DISPLAY PANEL - 1 mg Tablet Bottle Label