LYNAVOY

NDA 220295 · New Drug Application (NDA) Prescription

LINERIXIBAT

Sponsor (Drugs@FDA)
INTERCEPT Company: INTERCEPT PHARMACEUTICALS, INC.
First approved
Latest action

Drugs on HealthTrade

Drugs whose FDA actions or confirmed applications cite this number. A drug listed from this record shows “Not yet reviewed” on its page until an editor checks it.

Products

Drugs@FDA products under NDA 220295, with Orange Book listing details
ProductName and ingredientForm and strengthMarketing statusTE codeReferenceOrange Book
001 LYNAVOY LINERIXIBAT TABLET;ORAL 40MGPrescription– Reference listed drug, Reference standard RXApproved

Submissions

FDA submissions for NDA 220295, newest first
SubmissionStatusStatus dateReviewClassDocuments
Original 1ApprovedstandardType 1 - New Molecular EntityLetter for Original 1 (opens in a new tab)Label for Original 1 (opens in a new tab)

Orange Book patents

1 patent listed, as the Orange Book prints them.

Orange Book patents for NDA 220295
PatentExpiresClaimsUse codeSubmitted
9040518Product 001 Drug substance, Drug product –

Orange Book exclusivities

Orange Book exclusivities for NDA 220295
CodeProductExpires
NCE001
ODE-517001

Codes as the Orange Book prints them; its preface explains each code.

Prescription labels

The latest version of each DailyMed label, newest first. Indications and boxed warnings are cut to 1,000 characters; DailyMed has the full label.

  • Lynavoy

    LINERIXIBAT · Intercept Pharmaceuticals Inc · ORAL · Version 3 · effective

    Indications and usage

    1 INDICATIONS AND USAGE LYNAVOY is indicated for the treatment of cholestatic pruritus associated with primary biliary cholangitis (PBC) in adult patients. Limitations of Use Avoid use of LYNAVOY in patients with decompensated cirrhosis or those with prior or active hepatic decompensation events (e.g. variceal hemorrhage, ascites, hepatic encephalopathy) [see Use in Specific Populations (8.7) , Clinical Pharmacology (12.3) ] . LYNAVOY is an ileal bile acid transporter (IBAT) inhibitor indicated for the treatment of cholestatic pruritus associated with primary biliary cholangitis (PBC) in adult patients. ( 1 ) Limitations of Use Avoid use of LYNAVOY in patients with decompensated cirrhosis or those with prior or active hepatic decompensation events (e.g. variceal hemorrhage, ascites, hepatic encephalopathy). ( 1 )

    Full label on DailyMed for Lynavoy (opens in a new tab)

NDC products

1 product in the NDC directory with this application number.

NDC directory products for NDA 220295
Product NDCNameLabelerForm and routeCategoryMarketing dates
69516-140 in openFDA (opens in a new tab) Lynavoy LinerixibatIntercept Pharmaceuticals Inc TABLET, FILM COATED ORALNDA From

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Sources

Data provided by the U.S. Food and Drug Administration. Showing it here is not an FDA endorsement. openFDA asks: “Do not rely on openFDA to make decisions regarding medical care.”

Patent and exclusivity dates are as FDA lists them and can change. Nothing on this page is medical or investment advice.