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Lupin Obtains the US FDA Approval for Loteprednol Etabonate Ophthalmic Suspension

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Lupin Obtains the US FDA Approval for Loteprednol Etabonate Ophthalmic Suspension

Shots:

  • Lupin has obtained the US FDA approval for the ANDA of Loteprednol Etabonate Ophthalmic Suspension, 0.2%
  • The company’s approved generic is equivalent to the reference listed drug (RLD) of Bausch & Lomb’s Alrex Ophthalmic Suspension, 0.2% and will be manufactured at Pithampur (India)
  • The generic, Loteprednol Etabonate Ophthalmic Suspension, 0.2%, is approved for the providing temporary relief to the patients having symptoms of seasonal allergic conjunctivitis

Ref: Lupin | Image: Lupin

Related News:- Kala Pharmaceuticals' Eysuvis (loteprednol etabonate ophthalmic suspension) Receives US FDA's Approval for Dry Eye Disease

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Shivani Chandra

Shivani was a content writer at PharmaShots. She has a keen interest in recent innovations in the life sciences industry. She was covering news related to Product approvals, clinical trial results, and updates. We can be contacted at connect@pharmashots.com.

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