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Orange Book drug · Brand (NDA)

Romvimza

Vimseltinib

RLDNDA 219304 3 strengths Deciphera Pharms
Approved
Feb 14, 2025
Strengths
3
Listed patents
12

What does the FDA Orange Book show for Romvimza?

Romvimza contains Vimseltinib and is the new drug FDA Orange Book record for NDA 219304. The application has 3 presentations with strength, dosage-form, route, status, RLD/RS, TE, patent, and exclusivity context. Current inventory and clinical labeling are not established without an application-matched source.

FDA application
NDA 219304

New drug application identity from the Orange Book snapshot.

Application holder
Deciphera Pharmaceuticals LLC

The listed applicant holds the FDA application; this field does not establish the product manufacturer.

Product presentations
3

Each FDA product number remains tied to its own strength, dosage form, route, and status.

Marketing categories
Prescription

Orange Book marketing categories do not establish real-time inventory or commercial availability.

Reference roles
RLD / RS

RLD and RS designations are presentation-specific, not inferred from the trade name.

TE codes
None posted

Therapeutic-equivalence codes apply only within the matching Orange Book product heading.

Listed patents
12

A zero means none appear in this snapshot, not that no patent rights exist.

Exclusivity records
1

FDA exclusivity and listed patent protection are distinct regulatory concepts.

Sourced from the official FDA Orange Book data file · snapshot refreshed

FDA product-presentation matrix

Every product number in this exact application
Every FDA product presentation under this application, with strength, dosage form and route, marketing status, therapeutic-equivalence code, and reference role.
ProductStrengthDosage form / routeMarketing statusTE codeReference role
00114MGCAPSULEORALPrescriptionNone posted
RLD
00220MGCAPSULEORALPrescriptionNone posted
RLD
00330MGCAPSULEORALPrescriptionNone posted
RLDRS

Marketing status, TE code, RLD, and RS are presentation-level fields. Never transfer one product number's designation to another presentation.

Who is responsible for this application?

Application holder is not the same as manufacturer

FDA application holder

Deciphera Pharmaceuticals LLC

The Orange Book identifies this organization as the applicant responsible for NDA 219304.

Manufacturer status

Not established by the Orange Book

A product-specific FDA label or NDC source must independently identify a manufacturer, labeler, distributor, packager, repackager, or relabeler. The applicant name is not used as a substitute for that evidence.

Regulatory interpretation

What the record means, and what it does not
FDA marketing status

3 presentations listed as prescription

RX and OTC are Orange Book marketing categories, not real-time inventory signals. Confirm current commercial availability with labeling, the application holder, or an authoritative drug listing.

Therapeutic equivalence

No TE code is posted for this application

No TE code does not mean FDA found the product ineffective or non-equivalent. FDA generally publishes TE evaluations for multisource prescription products; single-source and some other products may have no code.

Patent & exclusivity record

12 listed patent expirations and 1 exclusivity date remain on or after Jul 26, 2026

The latest future date recorded across those files is Apr 30, 2045. Patent and FDA exclusivity operate independently, can overlap, and do not by themselves predict a generic launch date.

Same-ingredient landscape

0 other ANDAs and 0 other NDAs found

0 of the related ANDA applications are not marked discontinued. Sharing an ingredient does not establish pharmaceutical or therapeutic equivalence; strength, dosage form, route, and TE group still matter.

Which products are meaningfully comparable?

Exact ingredient + dosage form + route cohorts

NDA 219304 appears in 1 comparison cohort. These groups narrow the same-ingredient landscape, but strength and TE code must still match before interpreting therapeutic equivalence.

Capsule · Oral

Vimseltinib

1 application
Product rows
3
Active applications
1
Active with AB row
0

Why are clinical sections unavailable?

Exact application-label matching status
Exact source match queuedQueue NDA-219304

No exact application-level FDA or DailyMed label match has been reviewed for this application. Approved uses, dosing, warnings, adverse reactions, and clinical evidence remain unavailable rather than being inherited from a related brand, generic, or ingredient record.

Until an exact application match passes human review, this page intentionally omits approved uses, dosing, warnings, adverse reactions, mechanism, and clinical-study summaries. It never inherits those claims from an RLD, brand, generic, or same-ingredient product.

Strengths & dosage forms

3 approved presentations · NDA 219304
RLD
Strength
14MG
Dosage form
CAPSULE
Route
ORAL
Marketing status
Prescription

Key dates

Approval, patents, exclusivity

  1. Approval

    FDA approval date of this drug product.

    1 yr 6 mo ago

  2. Today

  3. Exclusivity ends · NCE

    New chemical entity exclusivity (5 years)

    in 3 yr 7 mo

  4. Patent 9181223 expires

    Listed drug substance patent expiration.

    in 7 yr 9 mo

  5. Patent 12285430 expires

    Listed method-of-use patent (U-4145) expiration.

    in 13 yr 7 mo

  6. Patent 12485120 expires

    Listed method-of-use patent (U-4145) expiration.

    in 13 yr 7 mo

  7. Patent 12582655 expires

    Listed method-of-use patent (U-4145) expiration.

    in 13 yr 7 mo

  8. Patent 11103507 expires

    Listed method-of-use patent (U-4145) expiration.

    in 13 yr 9 mo

  9. Patent 11679110 expires

    Listed method-of-use patent (U-4145) expiration.

    in 13 yr 9 mo

  10. Patent 12447149 expires

    Listed drug product patent expiration.

    in 18 yr 8 mo

  11. Patent 12528787 expires

    Listed drug substance patent expiration.

    in 18 yr 8 mo

  12. Patent 12551483 expires

    Listed drug product patent expiration.

    in 18 yr 8 mo

  13. Patent 12617775 expires

    Listed drug substance patent expiration.

    in 18 yr 8 mo

  14. Patent 12643883 expires

    Listed drug substance patent expiration.

    in 18 yr 8 mo

  15. Patent 12509443 expires

    Listed drug product patent expiration.

    in 19 yr

Patent & exclusivity timeline

Protection horizon
20262028203020322034203620382040204220442046TodayExclusivity NCE: 2030-02-14Exclusivity NCEPatent 9181223: 2034-03-14Patent 9181223Patent 12285430: 2039-12-23Patent 12285430Patent 12485120: 2039-12-23Patent 12485120Patent 12582655: 2039-12-23Patent 12582655Patent 11103507: 2040-02-03Patent 11103507Patent 11679110: 2040-02-03Patent 11679110Patent 12447149: 2044-12-06Patent 12447149Patent 12528787: 2044-12-06Patent 12528787Patent 12551483: 2044-12-06Patent 12551483Patent 12617775: 2044-12-06Patent 12617775Patent 12643883: 2044-12-06Patent 12643883Patent 12509443: 2045-04-30Patent 12509443
Patent expiryExclusivity endToday

Pharmaceutical detail

FDA product record

Active ingredient

VIMSELTINIB

Strength

14MG

Dosage form

CAPSULE

Route

ORAL

TE code

Not listed

Application

NDA 219304

Product number

001

Marketing status

Prescription

Reference listed drug (RLD)

Yes

Reference standard (RS)

No

Marketing exclusivity

Hatch-Waxman
  • NCENew chemical entity exclusivity (5 years)

    in 3 yr 7 mo

Listed patents

Orange Book patent file
Patents listed in the FDA Orange Book for this product, with expiration date and patent type.
PatentExpiresInType
9181223in 7 yr 9 mo
SubstanceProduct
12285430in 13 yr 7 mo
U-4145
12485120in 13 yr 7 mo
U-4145
12582655in 13 yr 7 mo
U-4145
11103507in 13 yr 9 mo
U-4145
11679110in 13 yr 9 mo
U-4145
12447149in 18 yr 8 mo
Product
12528787in 18 yr 8 mo
SubstanceProduct
12551483in 18 yr 8 mo
Product
12617775in 18 yr 8 mo
SubstanceProduct
12643883in 18 yr 8 mo
SubstanceProduct
12509443in 19 yr
Product

Active-ingredient family

Brand + generics

This is a reference-listed drug (RLD), the basis for generic (ANDA) applications. Other products sharing this ingredient are listed below.

No other applications share this active ingredient.

View full Vimseltinib family

How to use this record responsibly

Scope, limitations, and primary sources

What to verify before making a decision

  • The applicant is the holder of legal responsibility for the application; the Orange Book does not establish that the applicant manufactured or currently markets every listed product.
  • RX, OTC, and discontinued are FDA listing categories, not real-time pharmacy inventory or commercial-availability data.
  • Therapeutic equivalence applies only within the matching ingredient, dosage form, route, strength, and TE-code group; same ingredient alone is insufficient.
  • Listed patent and exclusivity dates are regulatory intelligence, not legal advice, a freedom-to-operate analysis, or a reliable generic-launch forecast.
  • The Orange Book is not prescribing information and does not provide indications, dosing, contraindications, adverse reactions, recalls, or current safety communications.

Official FDA references

Data shown here is normalized for search and comparison. When a regulatory, substitution, launch, or legal decision turns on a field, verify it against the current FDA record and the relevant source document.

Romvimza: frequently asked questions

Approval, therapeutic equivalence, patents, and exclusivity for this drug, from the FDA Orange Book.

Built directly from the FDA Orange Book product, patent, and exclusivity files refreshed Jul 02, 2026, 06:34 PM. Every strength of NDA 219304 is shown on this page. Interpret patents, exclusivity, availability, and therapeutic equivalence using the limitations above.

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