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MUMBAI, India & PRINCETON, N.J.–(BUSINESS WIRE)–Sun Biologic Industries Ltd. (Reuters: SUN.BO, Bloomberg: SUNP IN, NSE: SUNPHARMA, BSE: 524715, “Sun Pharma” and includes its subsidiaries and/or accessory companies) and Sun Pharma Advanced Research Aggregation Ltd. (Reuters: SPRC.BO, Bloomberg: SPADV IN, NSE: SPARC, BSE: 532872, “SPARC”) today appear U.S. Food and Drug Administering (USFDA) approval for the New Drug Application (NDA) of XELPROSTM (latanoprost ophthalmic emulsion) 0.005% for the abridgement of animated intraocular burden (IOP, or burden central the eye) in patients with open-angle glaucoma or ocular hypertension. This approval is from Sun Pharma’s Halol (Gujarat, India) facility.

Sun Pharma in-licensed XELPROSTM from SPARC in June 2015 and this approval will activate a anniversary acquittal to SPARC. SPARC is additionally acceptable for anniversary payments and royalties on commercialization of XELPROSTM in the US.

XELPROSTM is the aboriginal and alone anatomy of latanoprost that is not formulated with benzalkonium chloride (BAK), a bactericide frequently acclimated in contemporary ocular preparations. XELPROSTM is developed application SPARC’s proprietary Swollen Micelle Microemulsion (SMM) technology.

“As the alone BAK-free adaptation of latanoprost, XELPROSTM will be an important and another ysis advantage for individuals with open-angle glaucoma or ocular hypertension,” said Abhay Gandhi, CEO, North America, Sun Pharma. “This approval, advancing beneath than one ages afterward the approval of CEQUA™ (

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