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Orange Book drug · Brand (NDA)

Tasigna

Nilotinib Hydrochloride

RLDNDA 022068 3 strengths Novartis
Approved
Oct 29, 2007
Strengths
3
Listed patents
12

What does the FDA Orange Book show for Tasigna?

Tasigna contains Nilotinib Hydrochloride and is the new drug FDA Orange Book record for NDA 022068. 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 022068

New drug application identity from the Orange Book snapshot.

Application holder
Novartis Pharmaceuticals Corp

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
AB

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
2

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
001EQ 200MG BASECAPSULEORALPrescriptionAB
RLDRS
002EQ 150MG BASECAPSULEORALPrescriptionAB
RLD
003EQ 50MG BASECAPSULEORALPrescriptionAB
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

Novartis Pharmaceuticals Corp

The Orange Book identifies this organization as the applicant responsible for NDA 022068.

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

TE code AB across rated presentations

An AB code is an A-rating: FDA considers the product therapeutically equivalent to pharmaceutical equivalents in the same Orange Book heading and equivalence group.

Patent & exclusivity record

9 listed patent expirations and 2 exclusivity dates remain on or after Jul 26, 2026

The latest future date recorded across those files is Oct 07, 2032. Patent and FDA exclusivity operate independently, can overlap, and do not by themselves predict a generic launch date.

Same-ingredient landscape

5 other ANDAs and 0 other NDAs found

5 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 022068 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-022068

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 022068
TE ABRLDRS
Strength
EQ 200MG BASE
Dosage form
CAPSULE
Route
ORAL
Marketing status
Prescription

Key dates

Approval, patents, exclusivity

  1. Approval

    FDA approval date of this drug product.

    19 yr ago

  2. Patent 8389537 expires

    Listed method-of-use patent (U-1374) expiration.

    8 d ago

  3. Patent 8415363 expires

    Listed drug substance patent expiration.

    8 d ago

  4. Patent 8415363 expires

    Listed drug substance patent expiration.

    8 d ago

  5. Patent 8501760 expires

    Listed drug product patent expiration.

    8 d ago

  6. Today

  7. Patent 8389537*PED expires

    Listed listed patent expiration.

    in 6 mo

  8. Patent 8415363*PED expires

    Listed listed patent expiration.

    in 6 mo

  9. Patent 8501760*PED expires

    Listed listed patent expiration.

    in 6 mo

  10. Patent 8293756 expires

    Listed drug product patent expiration.

    in 1 yr 2 mo

  11. Patent 8293756*PED expires

    Listed listed patent expiration.

    in 1 yr 8 mo

  12. Patent 8163904 expires

    Listed drug substance patent expiration.

    in 2 yr 1 mo

  13. Exclusivity ends · ODE-380

    Orphan-drug exclusivity (7 years)

    in 2 yr 2 mo

  14. Patent 8163904*PED expires

    Listed listed patent expiration.

    in 2 yr 7 mo

  15. Exclusivity ends · PED

    Pediatric exclusivity (adds 6 months)

    in 2 yr 8 mo

  16. Patent 9061029 expires

    Listed drug substance patent expiration.

    in 5 yr 9 mo

  17. Patent 9061029 expires

    Listed drug substance patent expiration.

    in 5 yr 9 mo

  18. Patent 9061029*PED expires

    Listed listed patent expiration.

    in 6 yr 4 mo

Patent & exclusivity timeline

Protection horizon
20262027202820292030203120322033TodayPatent 8389537: 2026-07-18Patent 8389537Patent 8415363: 2026-07-18Patent 8415363Patent 8415363: 2026-07-18Patent 8415363Patent 8501760: 2026-07-18Patent 8501760Patent 8389537*PED: 2027-01-18Patent 8389537*PEDPatent 8415363*PED: 2027-01-18Patent 8415363*PEDPatent 8501760*PED: 2027-01-18Patent 8501760*PEDPatent 8293756: 2027-09-25Patent 8293756Patent 8293756*PED: 2028-03-25Patent 8293756*PEDPatent 8163904: 2028-08-23Patent 8163904Exclusivity ODE-380: 2028-09-23Exclusivity ODE-380Patent 8163904*PED: 2029-02-23Patent 8163904*PEDExclusivity PED: 2029-03-23Exclusivity PEDPatent 9061029: 2032-04-07Patent 9061029Patent 9061029: 2032-04-07Patent 9061029Patent 9061029*PED: 2032-10-07Patent 9061029*PED
Patent expiryExclusivity endToday

Pharmaceutical detail

FDA product record

Active ingredient

NILOTINIB HYDROCHLORIDE

Strength

EQ 200MG BASE

Dosage form

CAPSULE

Route

ORAL

TE code

AB

Application

NDA 022068

Product number

001

Marketing status

Prescription

Reference listed drug (RLD)

Yes

Reference standard (RS)

Yes

Marketing exclusivity

Hatch-Waxman
  • ODE-380Orphan-drug exclusivity (7 years)

    in 2 yr 2 mo

  • PEDPediatric exclusivity (adds 6 months)

    in 2 yr 8 mo

Listed patents

Orange Book patent file
Patents listed in the FDA Orange Book for this product, with expiration date and patent type.
PatentExpiresInType
83895378 d ago
U-1374
84153638 d ago
SubstanceProductU-1407
84153638 d ago
SubstanceProductU-1374
85017608 d ago
Product
8389537*PEDin 6 mo
8415363*PEDin 6 mo
8501760*PEDin 6 mo
8293756in 1 yr 2 mo
Product
8293756*PEDin 1 yr 8 mo
8163904in 2 yr 1 mo
SubstanceProduct
8163904*PEDin 2 yr 7 mo
9061029in 5 yr 9 mo
SubstanceU-1374
9061029in 5 yr 9 mo
SubstanceU-3231
9061029*PEDin 6 yr 4 mo

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 Nilotinib Hydrochloride 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.

Tasigna: 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 022068 is shown on this page. Interpret patents, exclusivity, availability, and therapeutic equivalence using the limitations above.

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