Skip to content
Assyro AI
Orange Book drug · Brand (NDA)

Phyrago

Dasatinib

RLDNDA 216099 6 strengths Handa Therap
Approved
Dec 05, 2023
Strengths
6
Listed patents
6

What does the FDA Orange Book show for Phyrago?

Phyrago contains Dasatinib and is the new drug FDA Orange Book record for NDA 216099. The application has 6 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 216099

New drug application identity from the Orange Book snapshot.

Application holder
Handa Therapeutics LLC

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

Product presentations
6

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
6

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
00120MGTABLETORALPrescriptionNone posted
RLD
00250MGTABLETORALPrescriptionNone posted
RLD
00370MGTABLETORALPrescriptionNone posted
RLD
00480MGTABLETORALPrescriptionNone posted
RLD
005100MGTABLETORALPrescriptionNone posted
RLDRS
006140MGTABLETORALPrescriptionNone posted
RLD

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

Handa Therapeutics LLC

The Orange Book identifies this organization as the applicant responsible for NDA 216099.

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

6 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

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

The latest future date recorded across those files is Jan 22, 2041. Patent and FDA exclusivity operate independently, can overlap, and do not by themselves predict a generic launch date.

Same-ingredient landscape

9 other ANDAs and 1 other NDA found

9 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 216099 appears in 1 comparison cohort. These groups narrow the same-ingredient landscape, but strength and TE code must still match before interpreting therapeutic equivalence.

Why are clinical sections unavailable?

Exact application-label matching status
Exact source match queuedQueue NDA-216099

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

6 approved presentations · NDA 216099
RLD
Strength
20MG
Dosage form
TABLET
Route
ORAL
Marketing status
Prescription

Key dates

Approval, patents, exclusivity

  1. Approval

    FDA approval date of this drug product.

    2 yr 8 mo ago

  2. Today

  3. Exclusivity ends · M-307

    New use / labeling-change exclusivity (3 years)

    in 4 mo

  4. Patent 11202778 expires

    Listed method-of-use patent (U-3770) expiration.

    in 14 yr 8 mo

  5. Patent 11202778 expires

    Listed method-of-use patent (U-3771) expiration.

    in 14 yr 8 mo

  6. Patent 11202778 expires

    Listed method-of-use patent (U-3772) expiration.

    in 14 yr 8 mo

  7. Patent 11298356 expires

    Listed drug product patent expiration.

    in 14 yr 8 mo

  8. Patent 11324745 expires

    Listed method-of-use patent (U-3767) expiration.

    in 14 yr 8 mo

  9. Patent 11324745 expires

    Listed method-of-use patent (U-3768) expiration.

    in 14 yr 8 mo

  10. Patent 11324745 expires

    Listed method-of-use patent (U-3769) expiration.

    in 14 yr 8 mo

  11. Patent 12433891 expires

    Listed method-of-use patent (U-3769) expiration.

    in 14 yr 8 mo

  12. Patent 12433891 expires

    Listed method-of-use patent (U-3768) expiration.

    in 14 yr 8 mo

  13. Patent 12433891 expires

    Listed method-of-use patent (U-3767) expiration.

    in 14 yr 8 mo

  14. Patent 12433891 expires

    Listed method-of-use patent (U-3770) expiration.

    in 14 yr 8 mo

  15. Patent 12433891 expires

    Listed method-of-use patent (U-3771) expiration.

    in 14 yr 8 mo

  16. Patent 12433891 expires

    Listed method-of-use patent (U-3772) expiration.

    in 14 yr 8 mo

  17. Patent 12465606 expires

    Listed drug product patent expiration.

    in 14 yr 8 mo

  18. Patent 12544376 expires

    Listed method-of-use patent (U-3767) expiration.

    in 14 yr 8 mo

  19. Patent 12544376 expires

    Listed method-of-use patent (U-3768) expiration.

    in 14 yr 8 mo

  20. Patent 12544376 expires

    Listed method-of-use patent (U-3769) expiration.

    in 14 yr 8 mo

  21. Patent 12544376 expires

    Listed method-of-use patent (U-3770) expiration.

    in 14 yr 8 mo

  22. Patent 12544376 expires

    Listed method-of-use patent (U-3771) expiration.

    in 14 yr 8 mo

  23. Patent 12544376 expires

    Listed method-of-use patent (U-3772) expiration.

    in 14 yr 8 mo

Patent & exclusivity timeline

Protection horizon
202620282030203220342036203820402042TodayExclusivity M-307: 2026-12-05Exclusivity M-307Patent 11202778: 2041-01-22Patent 11202778Patent 11202778: 2041-01-22Patent 11202778Patent 11202778: 2041-01-22Patent 11202778Patent 11298356: 2041-01-22Patent 11298356Patent 11324745: 2041-01-22Patent 11324745Patent 11324745: 2041-01-22Patent 11324745Patent 11324745: 2041-01-22Patent 11324745Patent 12433891: 2041-01-22Patent 12433891Patent 12433891: 2041-01-22Patent 12433891Patent 12433891: 2041-01-22Patent 12433891Patent 12433891: 2041-01-22Patent 12433891Patent 12433891: 2041-01-22Patent 12433891Patent 12433891: 2041-01-22Patent 12433891Patent 12465606: 2041-01-22Patent 12465606Patent 12544376: 2041-01-22Patent 12544376Patent 12544376: 2041-01-22Patent 12544376Patent 12544376: 2041-01-22Patent 12544376Patent 12544376: 2041-01-22Patent 12544376Patent 12544376: 2041-01-22Patent 12544376Patent 12544376: 2041-01-22Patent 12544376
Patent expiryExclusivity endToday

Pharmaceutical detail

FDA product record

Active ingredient

DASATINIB

Strength

20MG

Dosage form

TABLET

Route

ORAL

TE code

Not listed

Application

NDA 216099

Product number

001

Marketing status

Prescription

Reference listed drug (RLD)

Yes

Reference standard (RS)

No

Marketing exclusivity

Hatch-Waxman
  • M-307New use / labeling-change exclusivity (3 years)

    in 4 mo

Listed patents

Orange Book patent file
Patents listed in the FDA Orange Book for this product, with expiration date and patent type.
PatentExpiresInType
11202778in 14 yr 8 mo
U-3770
11202778in 14 yr 8 mo
U-3771
11202778in 14 yr 8 mo
U-3772
11298356in 14 yr 8 mo
Product
11324745in 14 yr 8 mo
U-3767
11324745in 14 yr 8 mo
U-3768
11324745in 14 yr 8 mo
U-3769
12433891in 14 yr 8 mo
U-3769
12433891in 14 yr 8 mo
U-3768
12433891in 14 yr 8 mo
U-3767
12433891in 14 yr 8 mo
U-3770
12433891in 14 yr 8 mo
U-3771
12433891in 14 yr 8 mo
U-3772
12465606in 14 yr 8 mo
Product
12544376in 14 yr 8 mo
U-3767
12544376in 14 yr 8 mo
U-3768
12544376in 14 yr 8 mo
U-3769
12544376in 14 yr 8 mo
U-3770
12544376in 14 yr 8 mo
U-3771
12544376in 14 yr 8 mo
U-3772

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.

View full Dasatinib 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.

Phyrago: 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 216099 is shown on this page. Interpret patents, exclusivity, availability, and therapeutic equivalence using the limitations above.

Related FDA reference tools

Agent CTA Background

Your Next Submission Could Take 6+ Fewer Weeks and Cost $250K Less.

Book a Demo