All FDA drug approvals

FDA approval · Drugs@FDA

APTIVUStipranavir

NDA021822 ·

FDA approved the original new drug application for APTIVUS on June 23, 2008, sponsored by BOEHRINGER INGELHEIM. FDA’s record shows no approved efficacy supplement on the application since.

Application
NDA021822
Sponsor
BOEHRINGER INGELHEIM
Original approval
Review
priority review
Submission class
Type 9 - New Indication Submitted as Distinct NDA, Consolidated with Original NDA after Approval
Active ingredient
tipranavir

Products under this application

Ingredient and strengthFormRouteMarketing status
tipranavir 100MG/MLSOLUTIONORALPrescription

Approved efficacy supplements

An efficacy supplement is how a sponsor asks FDA to approve a change that needs clinical evidence — most often a new indication. FDA’s record gives each one a submission number, a date and a review priority. It does not say what any supplement approved, so neither does this page. The approval letter and label for each are on accessdata.fda.gov under the application number.

FDA’s record shows no approved efficacy supplement on this application.

Source: FDA’s Drugs@FDA application file, via openFDA (export 2026-09-03). Every field on this page comes from that record.

An approval date is the start of the question, not the end

What a drug is worth to the company that owns it depends on what else is in the pipeline, how much cash is behind it and who else is running the same trial. FuzeBio reads a biotech end to end on demand — pipeline in plain English, trial design and endpoints, competitors, the cash position, and a valuation with its assumptions on the page. Moderna’s report is open in full, no account.

Open the Moderna report

A complete sample report — nothing held back, no sign-up.