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Orange Book drug · Brand (NDA)

Spravato

Esketamine Hydrochloride

RLDNDA 211243 Janssen Pharms
Approved
Mar 05, 2019
Strengths
1
Listed patents
7

What does the FDA Orange Book show for Spravato?

Spravato contains Esketamine Hydrochloride and is the new drug FDA Orange Book record for NDA 211243. The application has 1 presentation 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 211243

New drug application identity from the Orange Book snapshot.

Application holder
Janssen Pharmaceuticals Inc

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

Product presentations
1

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
7

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
001EQ 28MG BASESPRAYNASALPrescriptionNone 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

Janssen Pharmaceuticals Inc

The Orange Book identifies this organization as the applicant responsible for NDA 211243.

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

1 presentation 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

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

The latest future date recorded across those files is Feb 18, 2040. 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 211243 appears in 1 comparison cohort. These groups narrow the same-ingredient landscape, but strength and TE code must still match before interpreting therapeutic equivalence.

Spray · Nasal

Esketamine Hydrochloride

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

Why are clinical sections unavailable?

Exact application-label matching status
Exact source match queuedQueue NDA-211243

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.

Product detail

NDA 211243
RLDRS
Strength
EQ 28MG BASE
Dosage form
SPRAY
Route
NASAL
Marketing status
Prescription

Key dates

Approval, patents, exclusivity

  1. Approval

    FDA approval date of this drug product.

    7 yr 6 mo ago

  2. Today

  3. Patent 9592207 expires

    Listed method-of-use patent (U-2502) expiration.

    in 8 mo

  4. Patent 9592207 expires

    Listed method-of-use patent (U-4112) expiration.

    in 8 mo

  5. Exclusivity ends · I-959

    New indication exclusivity (3 years)

    in 1 yr 6 mo

  6. Patent 8785500 expires

    Listed method-of-use patent (U-2502) expiration.

    in 6 yr 8 mo

  7. Patent 8785500 expires

    Listed method-of-use patent (U-4112) expiration.

    in 6 yr 8 mo

  8. Patent 11446260 expires

    Listed method-of-use patent (U-4118) expiration.

    in 7 yr 9 mo

  9. Patent 11446260 expires

    Listed method-of-use patent (U-4119) expiration.

    in 7 yr 9 mo

  10. Patent 11446260 expires

    Listed method-of-use patent (U-3444) expiration.

    in 7 yr 9 mo

  11. Patent 11446260 expires

    Listed method-of-use patent (U-3445) expiration.

    in 7 yr 9 mo

  12. Patent 11446260 expires

    Listed method-of-use patent (U-3446) expiration.

    in 7 yr 9 mo

  13. Patent 10869844 expires

    Listed method-of-use patent (U-4113) expiration.

    in 9 yr 3 mo

  14. Patent 10869844 expires

    Listed method-of-use patent (U-4114) expiration.

    in 9 yr 3 mo

  15. Patent 10869844 expires

    Listed method-of-use patent (U-3035) expiration.

    in 9 yr 3 mo

  16. Patent 10869844 expires

    Listed method-of-use patent (U-3034) expiration.

    in 9 yr 3 mo

  17. Patent 10869844 expires

    Listed method-of-use patent (U-3036) expiration.

    in 9 yr 3 mo

  18. Patent 11173134 expires

    Listed method-of-use patent (U-4115) expiration.

    in 9 yr 3 mo

  19. Patent 11173134 expires

    Listed method-of-use patent (U-3536) expiration.

    in 9 yr 3 mo

  20. Patent 11173134 expires

    Listed method-of-use patent (U-3257) expiration.

    in 9 yr 3 mo

  21. Patent 11311500 expires

    Listed method-of-use patent (U-4116) expiration.

    in 9 yr 3 mo

  22. Patent 11311500 expires

    Listed method-of-use patent (U-4117) expiration.

    in 9 yr 3 mo

  23. Patent 11311500 expires

    Listed method-of-use patent (U-3034) expiration.

    in 9 yr 3 mo

  24. Patent 11311500 expires

    Listed method-of-use patent (U-3036) expiration.

    in 9 yr 3 mo

  25. Patent 11311500 expires

    Listed method-of-use patent (U-3035) expiration.

    in 9 yr 3 mo

  26. Patent 11883526 expires

    Listed method-of-use patent (U-4120) expiration.

    in 13 yr 9 mo

  27. Patent 11883526 expires

    Listed method-of-use patent (U-3812) expiration.

    in 13 yr 9 mo

  28. Patent 11883526 expires

    Listed method-of-use patent (U-3813) expiration.

    in 13 yr 9 mo

Patent & exclusivity timeline

Protection horizon
20262028203020322034203620382040TodayPatent 9592207: 2027-03-20Patent 9592207Patent 9592207: 2027-03-20Patent 9592207Exclusivity I-959: 2028-01-17Exclusivity I-959Patent 8785500: 2033-03-05Patent 8785500Patent 8785500: 2033-03-05Patent 8785500Patent 11446260: 2034-03-14Patent 11446260Patent 11446260: 2034-03-14Patent 11446260Patent 11446260: 2034-03-14Patent 11446260Patent 11446260: 2034-03-14Patent 11446260Patent 11446260: 2034-03-14Patent 11446260Patent 10869844: 2035-09-10Patent 10869844Patent 10869844: 2035-09-10Patent 10869844Patent 10869844: 2035-09-10Patent 10869844Patent 10869844: 2035-09-10Patent 10869844Patent 10869844: 2035-09-10Patent 10869844Patent 11173134: 2035-09-10Patent 11173134Patent 11173134: 2035-09-10Patent 11173134Patent 11173134: 2035-09-10Patent 11173134Patent 11311500: 2035-09-10Patent 11311500Patent 11311500: 2035-09-10Patent 11311500Patent 11311500: 2035-09-10Patent 11311500Patent 11311500: 2035-09-10Patent 11311500Patent 11311500: 2035-09-10Patent 11311500Patent 11883526: 2040-02-18Patent 11883526Patent 11883526: 2040-02-18Patent 11883526Patent 11883526: 2040-02-18Patent 11883526
Patent expiryExclusivity endToday

Pharmaceutical detail

FDA product record

Active ingredient

ESKETAMINE HYDROCHLORIDE

Strength

EQ 28MG BASE

Dosage form

SPRAY

Route

NASAL

TE code

Not listed

Application

NDA 211243

Product number

001

Marketing status

Prescription

Reference listed drug (RLD)

Yes

Reference standard (RS)

Yes

Marketing exclusivity

Hatch-Waxman
  • I-959New indication exclusivity (3 years)

    in 1 yr 6 mo

Listed patents

Orange Book patent file
Patents listed in the FDA Orange Book for this product, with expiration date and patent type.
PatentExpiresInType
9592207in 8 mo
U-2502
9592207in 8 mo
U-4112
8785500in 6 yr 8 mo
U-2502
8785500in 6 yr 8 mo
U-4112
11446260in 7 yr 9 mo
U-4118
11446260in 7 yr 9 mo
U-4119
11446260in 7 yr 9 mo
U-3444
11446260in 7 yr 9 mo
U-3445
11446260in 7 yr 9 mo
U-3446
10869844in 9 yr 3 mo
U-4113
10869844in 9 yr 3 mo
U-4114
10869844in 9 yr 3 mo
U-3035
10869844in 9 yr 3 mo
U-3034
10869844in 9 yr 3 mo
U-3036
11173134in 9 yr 3 mo
U-4115
11173134in 9 yr 3 mo
U-3536
11173134in 9 yr 3 mo
U-3257
11311500in 9 yr 3 mo
U-4116
11311500in 9 yr 3 mo
U-4117
11311500in 9 yr 3 mo
U-3034
11311500in 9 yr 3 mo
U-3036
11311500in 9 yr 3 mo
U-3035
11883526in 13 yr 9 mo
U-4120
11883526in 13 yr 9 mo
U-3812
11883526in 13 yr 9 mo
U-3813

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 Esketamine 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.

Spravato: 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 211243 is shown on this page. Interpret patents, exclusivity, availability, and therapeutic equivalence using the limitations above.

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