USFDA Approves Strides Pharma's Generic Fluoxetine Tablets for Enhanced Dosing Flexibility

Monday, 16 September 2024, 03:05

USFDA approval marks a significant stride for Strides Pharma as it launches generic Fluoxetine tablets, enhancing patient access to this vital antidepressant. TWi Pharmaceuticals' equivalent product sets a new benchmark in the fluoxetine market, promising improved dosing flexibility from their Puducherry facility.
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USFDA Approves Strides Pharma's Generic Fluoxetine Tablets for Enhanced Dosing Flexibility

USFDA Approval for Strides Pharma

Strides Pharma Science Ltd's subsidiary has achieved a significant milestone with the USFDA approval of its generic Fluoxetine tablets (60 mg). These tablets are designed to be equivalent to TWi Pharmaceuticals' version, ensuring competitive presence in the antidepressant market.

Details of the Approval

  • Product: Generic Fluoxetine Tablets
  • Strength: 60 mg
  • Production Facility: Puducherry
  • Market Impact: Enhanced competition in the fluoxetine sector

Implications for Patients

The launch of this generic medication is poised to provide greater dosing flexibility for patients relying on antidepressants, aligning with IMS data trends observed in antidepressant usage.


This article was prepared using information from open sources in accordance with the principles of Ethical Policy. The editorial team is not responsible for absolute accuracy, as it relies on data from the sources referenced.


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