Lupin launches Loteprednol Etabonate ophthalmic suspension 0.5% in US
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Lupin launches Loteprednol Etabonate ophthalmic suspension 0.5% in US

Loteprednol Etabonate Ophthalmic Suspension, 0.5% is indicated for the treatment of steroidresponsive inflammatory conditions of the palpebral and bulbar conjunctiva

  • By IPP Bureau | July 17, 2025

Global pharma major Lupin Limited (Lupin) announced the launch of Loteprednol Etabonate Ophthalmic Suspension, 0.5%, in the United States. Loteprednol Etabonate Ophthalmic Suspension, 0.5% is bioequivalent to Lotemax Ophthalmic Suspension, 0.5%, of Bausch & Lomb.

Loteprednol Etabonate Ophthalmic Suspension, 0.5% is indicated for the treatment of steroidresponsive inflammatory conditions of the palpebral and bulbar conjunctiva, cornea and anterior segment of the globe such as allergic conjunctivitis, acne rosacea, superficial punctate keratitis, herpes zoster keratitis, iritis, cyclitis, selected infective conjunctivitides, when the inherent hazard of steroid use is accepted to obtain an advisable diminution in edema and inflammation.

It is also indicated for the treatment of post-operative inflammation following ocular surgery. Loteprednol Etabonate Ophthalmic Suspension (RLD Lotemax) had estimated annual sales of US$ 55 million in the U.S. (IQVIA MAT May 2025).

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