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When Did Latisse Go Generic? The Arrival of Bimatoprost

3 min read

While Latisse was first approved by the FDA in December 2008 [1.6.1], the answer to when did Latisse go generic is more complex. The first generic approvals appeared years before the final patents expired in 2024, offering a more affordable option for treating eyelash hypotrichosis [1.2.1, 1.2.3].

Quick Summary

Generic versions of Latisse, known as bimatoprost ophthalmic solution 0.03%, became available as early as 2016, with more following as patents expired through May 2024. These generics offer the same FDA-approved efficacy at a lower cost.

Key Points

  • First Generic Approval: The first FDA approval for a generic version of Latisse (bimatoprost 0.03%) was granted as early as December 2014 [1.2.3].

  • Patent Expiration: Key patents for Latisse, which protected it from widespread generic competition, expired by May 2024, allowing more generic versions to enter the market [1.2.1, 1.3.2].

  • Same Active Ingredient: Generic bimatoprost contains the exact same active ingredient at the same concentration as brand-name Latisse and is considered equally effective by the FDA [1.4.7].

  • Significant Cost Savings: The primary benefit of the generic version is its lower cost, often available for less than a third of the price of brand-name Latisse [1.5.2, 1.5.4].

  • Prescription Required: Both Latisse and its generic counterparts are prescription medications and are not available over the counter [1.4.7].

  • Mechanism of Action: Bimatoprost works by extending the growth phase (anagen phase) of the eyelash cycle and increasing the number of hairs that grow, leading to longer, thicker lashes [1.4.5, 1.7.1].

  • Side Effects are Identical: Potential side effects, such as eye redness, eyelid skin darkening, and a rare risk of permanent iris color change, are the same for both the brand and generic versions [1.8.3, 1.8.4].

In This Article

The Journey from Glaucoma Treatment to Eyelash Enhancer

Latisse's active ingredient, bimatoprost, was first used in a medicated eye drop called Lumigan, approved in 2001 to treat high eye pressure (ocular hypertension) and glaucoma [1.2.7, 1.6.4]. Patients using Lumigan reported a noticeable side effect: their eyelashes were growing longer, thicker, and darker [1.6.4]. This discovery prompted Allergan, the manufacturer, to study bimatoprost specifically for eyelash growth. After clinical trials, the FDA approved Latisse on December 24, 2008, for the treatment of hypotrichosis, the medical term for having inadequate eyelashes [1.6.1, 1.6.5].

Understanding Latisse's Patent and Generic Availability

The question of when did Latisse go generic? involves patent law and FDA approvals. A drug's patent protects it from generic competition for a set period [1.3.5]. Latisse was protected by multiple patents covering its formulation and method of use [1.2.1, 1.3.2]. While some patents were set to expire as late as May 2024, generic manufacturers can challenge these patents [1.2.2, 1.3.2].

The FDA granted approval to several companies to market generic bimatoprost ophthalmic solution 0.03% well before all of Latisse's patents expired. For instance, Apotex received approval in December 2014, and Sandoz launched its generic version in December 2016 [1.2.3, 1.2.5]. The final key patents for Latisse expired in May 2024, opening the market for more generic competition [1.3.2, 1.2.1].

How Bimatoprost Promotes Eyelash Growth

Bimatoprost is a prostaglandin analog, a synthetic compound that mimics naturally occurring substances in the body [1.7.1, 1.4.7]. It is believed to work by interacting with prostaglandin receptors in the hair follicles [1.7.3]. This interaction affects the eyelash growth cycle in two main ways:

  1. It increases the duration of the growth (anagen) phase: This allows eyelashes to grow longer than they normally would [1.4.5, 1.7.4].
  2. It increases the number of hairs that sprout during the growth phase: This results in fuller, thicker lashes [1.7.1, 1.7.6].

Clinical studies have shown significant results after 16 weeks of daily use, with users experiencing lashes that are up to 25% longer, 106% fuller, and 18% darker [1.4.5, 1.4.6]. If you stop using bimatoprost, your eyelashes will gradually return to their previous appearance over several weeks to months [1.7.1].

Brand Name vs. Generic: A Comparison

Generic bimatoprost 0.03% is FDA-approved and considered bioequivalent to Latisse, meaning it has the same active ingredient, strength, and efficacy [1.4.7]. The primary differences for consumers are cost and branding.

Feature Latisse (Brand Name) Bimatoprost (Generic)
Active Ingredient Bimatoprost 0.03% [1.4.2] Bimatoprost 0.03% [1.4.7]
FDA Approved Yes, for hypotrichosis [1.6.1] Yes, for hypotrichosis [1.4.1]
Efficacy Clinically proven for length, thickness, and darkness [1.4.6] Same clinical efficacy as the brand name [1.4.7]
Application Once daily to the base of upper eyelashes with a sterile applicator [1.7.1] Once daily to the base of upper eyelashes with a sterile applicator [1.4.6]
Cost (approx.) $130–$150 per 3-5 mL bottle [1.5.4, 1.5.5] As low as $35–$60 per 3-5 mL bottle [1.5.2, 1.5.6]
Prescription Required Yes [1.4.3] Yes [1.4.7]

Potential Side Effects and Safety Considerations

Both Latisse and generic bimatoprost have the same potential side effects. The most common ones, occurring in about 3-4% of users, include itchy or red eyes and darkening of the eyelid skin at the application site [1.8.3, 1.6.6].

Other less common but important side effects include:

  • Dry eyes and eye irritation [1.8.3].
  • Permanent darkening of the iris: This is rare but may cause the colored part of the eye to turn more brown over months or years [1.8.4].
  • Hair growth outside the treatment area: If the solution regularly drips onto other skin, it can cause hair to grow there. It is important to blot away any excess solution [1.7.1, 1.8.5].

Before using bimatoprost, you should remove contact lenses and put them back in 15 minutes after application [1.7.1]. It's crucial to use the provided sterile, single-use applicators to prevent eye infections [1.4.7]. You should discuss your full medical history with your doctor, especially if you have eye conditions like glaucoma or uveitis [1.7.3].

Conclusion

Generic versions of Latisse have been available for several years, with the first approvals dating back to 2014 and 2016 [1.2.3, 1.2.5]. With the final patents expiring in May 2024, access to affordable, FDA-approved generic bimatoprost has increased significantly [1.2.1]. This allows more individuals to use this proven treatment for eyelash hypotrichosis, achieving the same results as the brand name product but at a fraction of the cost. As with any prescription medication, it is essential to consult with a healthcare provider to ensure it is the right choice for you and to use it as directed to maximize benefits and minimize risks. For more authoritative information on prescription drugs, you can visit the FDA's website.

Frequently Asked Questions

Yes, generic bimatoprost ophthalmic solution 0.03% is considered by the FDA to be equally safe and effective as brand-name Latisse. They both contain the same active ingredient in the same concentration [1.4.7].

The price can vary, but generic bimatoprost is significantly cheaper than Latisse. It can be found for as low as $35–$60 for a one-month supply, while the brand name often costs between $130 and $150 [1.5.2, 1.5.4].

Yes, both brand-name Latisse and its generic version, bimatoprost ophthalmic solution 0.03%, require a prescription from a licensed healthcare provider [1.4.7].

Latisse was first approved by the U.S. Food and Drug Administration (FDA) on December 24, 2008, for the treatment of hypotrichosis of the eyelashes [1.6.1, 1.6.2].

The active ingredient in both Latisse and its generic version is bimatoprost, at a concentration of 0.03% [1.4.2, 1.4.7].

The most common side effects, affecting approximately 3-4% of users, are itchy eyes, eye redness, and darkening of the eyelid skin where the product is applied [1.8.3, 1.6.6].

Yes, this is a rare but possible side effect. Bimatoprost can cause increased brown pigmentation in the iris (the colored part of the eye), and this change is likely to be permanent [1.8.4, 1.4.3].

References

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  5. 5
  6. 6
  7. 7
  8. 8
  9. 9
  10. 10
  11. 11
  12. 12
  13. 13
  14. 14
  15. 15
  16. 16
  17. 17
  18. 18
  19. 19
  20. 20
  21. 21
  22. 22
  23. 23
  24. 24
  25. 25
  26. 26
  27. 27

Medical Disclaimer

This content is for informational purposes only and should not replace professional medical advice.