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Orange Book drug · Brand (NDA)

Auvi-q

Epinephrine

RLDNDA 201739 3 strengths Kaleo Inc
Approved
Aug 10, 2012
Strengths
3
Listed patents
9

What does the FDA Orange Book show for Auvi-q?

Auvi-q contains Epinephrine and is the new drug FDA Orange Book record for NDA 201739. 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 201739

New drug application identity from the Orange Book snapshot.

Application holder
Kaleo Inc

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
BX

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

Listed patents
9

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

Exclusivity records
0

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 0.3MG/DELIVERYSOLUTIONINTRAMUSCULAR, SUBCUTANEOUSPrescriptionBX
RLD
002EQ 0.15MG/DELIVERYSOLUTIONINTRAMUSCULAR, SUBCUTANEOUSPrescriptionBX
RLDRS
003EQ 0.1MG/DELIVERYSOLUTIONINTRAMUSCULAR, SUBCUTANEOUSPrescriptionNone 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

Kaleo Inc

The Orange Book identifies this organization as the applicant responsible for NDA 201739.

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 BX across rated presentations

A BX code is a B-rating: FDA does not consider the product therapeutically equivalent to other pharmaceutical equivalents in its heading at this time. 1 presentation in the application has no posted TE code.

Patent & exclusivity record

9 listed patent expirations and 0 exclusivity dates remain on or after Jul 26, 2026

The latest future date recorded across those files is Dec 21, 2037. Patent and FDA exclusivity operate independently, can overlap, and do not by themselves predict a generic launch date.

Same-ingredient landscape

11 other ANDAs and 16 other NDAs 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 201739 appears in 1 comparison cohort. These groups narrow the same-ingredient landscape, but strength and TE code must still match before interpreting therapeutic equivalence.

Solution · Intramuscular, Subcutaneous

Epinephrine

2 applications
Product rows
5
Active applications
2
Active with AB row
0
Symjepi · NDA 207534

Why are clinical sections unavailable?

Exact application-label matching status
Exact source match queuedQueue NDA-201739

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 201739
TE BXRLD
Strength
EQ 0.3MG/DELIVERY
Dosage form
SOLUTION
Route
INTRAMUSCULAR, SUBCUTANEOUS
Marketing status
Prescription

Key dates

Approval, patents, exclusivity

  1. Approval

    FDA approval date of this drug product.

    14 yr 2 mo ago

  2. Today

  3. Patent 11590286 expires

    Listed drug product patent expiration.

    in 5 mo

  4. Patent 8206360 expires

    Listed drug product patent expiration.

    in 7 mo

  5. Patent 7947017 expires

    Listed drug product patent expiration.

    in 1 yr 8 mo

  6. Patent 8231573 expires

    Listed drug product patent expiration.

    in 2 yr 4 mo

  7. Patent 8226610 expires

    Listed drug product patent expiration.

    in 2 yr 9 mo

  8. Patent 8021344 expires

    Listed drug product patent expiration.

    in 3 yr 4 mo

Patent & exclusivity timeline

Protection horizon
20262027202820292030TodayPatent 11590286: 2026-12-12Patent 11590286Patent 8206360: 2027-02-27Patent 8206360Patent 7947017: 2028-03-12Patent 7947017Patent 8231573: 2028-11-25Patent 8231573Patent 8226610: 2029-04-10Patent 8226610Patent 8021344: 2029-11-02Patent 8021344
Patent expiryExclusivity endToday

Pharmaceutical detail

FDA product record

Active ingredient

EPINEPHRINE

Strength

EQ 0.3MG/DELIVERY

Dosage form

SOLUTION

Route

INTRAMUSCULAR, SUBCUTANEOUS

TE code

BX

Application

NDA 201739

Product number

001

Marketing status

Prescription

Reference listed drug (RLD)

Yes

Reference standard (RS)

No

Listed patents

Orange Book patent file
Patents listed in the FDA Orange Book for this product, with expiration date and patent type.
PatentExpiresInType
11590286in 5 mo
Product
8206360in 7 mo
Product
7947017in 1 yr 8 mo
Product
8231573in 2 yr 4 mo
Product
8226610in 2 yr 9 mo
Product
8021344in 3 yr 4 mo
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.

View full Epinephrine 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.

Auvi-q: 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 201739 is shown on this page. Interpret patents, exclusivity, availability, and therapeutic equivalence using the limitations above.

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