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Last Updated: April 26, 2024

DrugPatentWatch Database Updates: New Patent Additions


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DrugPatentWatch Database Updates: New Patent Additions

These are patents which have been reported by the FDA since the last major update; they are not yet in the main database.
Applicant Tradename Generic Name Dosage NDA Number Approval Date Type RLD Patent No. Product Substance Delist Requested Patent Expiration Date Submitted Usecode Patented / Exclusive Use
Esperion Theraps Inc NEXLIZET bempedoic acid; ezetimibe TABLET 211617 001 Feb 26, 2020 RX Yes ⤷  Try a Trial ⤷  Try a Trial 2021-10-14 U-3224 A METHOD OF TREATING HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA OR ESTABLISHED ATHEROSCLEROTIC CARDIOVASCULAR DISEASE BY DECREASING THE LEVEL OF LDL-C USING A FIXED DOSE COMBINATION OF 180 MG BEMPEDOIC ACID AND 10 MG EZETIMIBE
Esperion Theraps Inc NEXLIZET bempedoic acid; ezetimibe TABLET 211617 001 Feb 26, 2020 RX Yes ⤷  Try a Trial ⤷  Try a Trial 2021-10-14 U-3884 A METHOD OF LOWERING LDL-C OR REDUCING THE RISK OF CARDIOVASCULAR DISEASE IN PATIENTS WITH FAMILIAL HYPERCHOLESTEROLEMIA USING A FIXED-DOSE COMBINATION OF 180 MG BEMPEDOIC ACID AND 10 MG EZETIMIBE
Esperion Theraps Inc NEXLIZET bempedoic acid; ezetimibe TABLET 211617 001 Feb 26, 2020 RX Yes ⤷  Try a Trial ⤷  Try a Trial 2023-10-03 U-3692 A METHOD OF TREATING HETEROZYGOUS FAMILIAL HYPERCHOLESTEROLEMIA OR ESTABLISHED ATHEROSCLEROTIC CARDIOVASCULAR DISEASE BY DECREASING THE LEVEL OF LDL-C USING 180 MG BEMPEDOIC ACID AND 10 MG EZETIMIBE
Esperion Theraps Inc NEXLIZET bempedoic acid; ezetimibe TABLET 211617 001 Feb 26, 2020 RX Yes ⤷  Try a Trial ⤷  Try a Trial 2023-10-03 U-3883 A METHOD OF LOWERING LDL-C OR REDUCING THE RISK OF CARDIOVASCULAR DISEASE IN PATIENTS WITH FAMILIAL HYPERCHOLESTEROLEMIA USING 180 MG BEMPEDOIC ACID AND 10 MG EZETIMIBE
Blueprint Medicines AYVAKIT avapritinib TABLET 212608 004 Jun 16, 2021 RX Yes ⤷  Try a Trial Y Y ⤷  Try a Trial 2024-04-23
Blueprint Medicines AYVAKIT avapritinib TABLET 212608 005 Jun 16, 2021 RX Yes ⤷  Try a Trial Y Y ⤷  Try a Trial 2024-04-23
>Applicant >Tradename >Generic Name >Dosage >NDA >Number >Approval Date >Type >RLD >Patent No. >Product >Substance >Delist Requested >Patent Expiration >Usecode >Patented / Exclusive Use

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