Page updated ·next FDA decision on the calendar·Data as of Oct 11, 2026 9:31 PM ET
MR-107A-02 (fast-acting meloxicam) is a Viatris Inc. program in moderate-to-severe acute pain (non-opioid). Its PDUFA date is Dec 27, 2026, the FDA's goal date to complete review of the application. Every date links its source.
Indication under review: Moderate-to-severe acute pain (non-opioid). Sponsor: Viatris Inc. (VTRS). Market-cap tier at the time we tracked it: Large. We track 1 catalyst event for this program: 1 upcoming and 0 in the record. A PDUFA date is the FDA's target date to complete review of a marketing application; a readout is the sponsor's expected date for clinical trial results. What a PDUFA date is · why we do not compare trial results across drugs.
When is MR-107A-02 (fast-acting meloxicam)'s next FDA decision or readout?
MR-107A-02 (fast-acting meloxicam)'s PDUFA date is Dec 27, 2026. That is the FDA's goal date to complete review of the application; the agency can act earlier or extend it.
What happened at MR-107A-02 (fast-acting meloxicam)'s most recent FDA decision?
No FDA decision for MR-107A-02 (fast-acting meloxicam) is in our archive yet.
What is MR-107A-02 (fast-acting meloxicam) used for?
In our records MR-107A-02 (fast-acting meloxicam) is under review or in development for Moderate-to-severe acute pain (non-opioid).
Who makes MR-107A-02 (fast-acting meloxicam)?
Viatris Inc. (VTRS).
Where does this data come from?
FDA announcements, sponsor press releases and SEC filings; every date on this page links its source.
Facts and dates only; not investment advice. Verify against primary FDA, SEC
and company filings. pdufa.bio is not affiliated with the FDA.
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