ACULAR (ketorolac tromethamine) by AbbVie is anti-inflammatory drug which, when administered systemically, has demonstrated analgesic, anti-inflammatory, and anti-pyretic activity. First approved in 1992.
Drug data last refreshed 1h ago · AI intelligence enriched 4h ago
ACULAR (ketorolac tromethamine) is a nonsteroidal anti-inflammatory drug (NSAID) administered as an ophthalmic solution for topical eye use. It reduces inflammation and provides analgesia by inhibiting prostaglandin biosynthesis. The drug is indicated for ocular pain and inflammation associated with allergic conjunctivitis, post-operative inflammation, and other ophthalmic conditions.
Product is nearing loss of exclusivity with modest Part D claims, indicating a contracting commercial footprint and potential team rationalization.
anti-inflammatory drug which, when administered systemically, has demonstrated analgesic, anti-inflammatory, and anti-pyretic activity. The mechanism of its action is thought to be due to its ability to inhibit prostaglandin biosynthesis.
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Study of CU06-1004 in Patients With Daibetic Macular Edema
A First-in-human Trial of SZN-8141 in Diabetic Macular Edema
Phase 3 Study of Intravitreal OLN324 in Adults With Neovascular (Wet) Age-related Macular Degeneration (nAMD) (OLN324-CP-05)
Phase 3 Study of Intravitreal OLN324 in Adults With Neovascular (Wet) Age-related Macular Degeneration (nAMD) (OLN324-CP-04)
A Clinical Trial of MK-8748 Compared to Aflibercept in Participants With Diabetic Macular Edema (MK-8748-005)
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The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.
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Upgrade to Pro — $25/moWorking on ACULAR offers limited career growth given its LOE Approaching status and minimal linked job openings. This role is best suited for professionals seeking a stable, lower-intensity assignment or those transitioning between growth-stage products, as the focus shifts from launch and expansion to defending market share against generics.