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Orange Book drug · Brand (NDA)

Crexont

Carbidopa; Levodopa

RLDNDA 217186 4 strengths Impax
Approved
Aug 07, 2024
Strengths
4
Listed patents
29

What does the FDA Orange Book show for Crexont?

Crexont contains Carbidopa; Levodopa and is the new drug FDA Orange Book record for NDA 217186. The application has 4 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 217186

New drug application identity from the Orange Book snapshot.

Application holder
Impax Laboratories LLC

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

Product presentations
4

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
29

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
00135MG;140MGCAPSULE, EXTENDED RELEASEORALPrescriptionNone posted
RLD
00252.5MG;210MGCAPSULE, EXTENDED RELEASEORALPrescriptionNone posted
RLD
00370MG;280MGCAPSULE, EXTENDED RELEASEORALPrescriptionNone posted
RLD
00487.5MG;350MGCAPSULE, EXTENDED RELEASEORALPrescriptionNone 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

Impax Laboratories LLC

The Orange Book identifies this organization as the applicant responsible for NDA 217186.

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

4 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

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

The latest future date recorded across those files is Dec 21, 2041. Patent and FDA exclusivity operate independently, can overlap, and do not by themselves predict a generic launch date.

Same-ingredient landscape

31 other ANDAs and 5 other NDAs found

17 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 217186 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, Extended Release · Oral

Carbidopa; Levodopa

2 applications
Product rows
8
Active applications
2
Active with AB row
0

Why are clinical sections unavailable?

Exact application-label matching status
Exact source match queuedQueue NDA-217186

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

4 approved presentations · NDA 217186
RLD
Strength
35MG;140MG
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Marketing status
Prescription

Key dates

Approval, patents, exclusivity
  1. Approval

    FDA approval date of this drug product.

    2 yr ago

  2. Today

  3. Exclusivity ends · NP

    New product exclusivity (3 years)

    in 1 yr 1 mo

  4. Patent 10098845 expires

    Listed drug product patent expiration.

    in 8 yr 4 mo

  5. Patent 10292935 expires

    Listed drug product patent expiration.

    in 8 yr 4 mo

  6. Patent 10688058 expires

    Listed drug product patent expiration.

    in 8 yr 4 mo

  7. Patent 10973769 expires

    Listed drug product patent expiration.

    in 8 yr 4 mo

  8. Patent 10987313 expires

    Listed drug product patent expiration.

    in 8 yr 4 mo

  9. Patent 11357733 expires

    Listed drug product patent expiration.

    in 8 yr 4 mo

  10. Patent 11622941 expires

    Listed drug product patent expiration.

    in 8 yr 4 mo

  11. Patent 11666538 expires

    Listed drug product patent expiration.

    in 8 yr 4 mo

  12. Patent 12064521 expires

    Listed drug product patent expiration.

    in 8 yr 4 mo

  13. Patent 12128141 expires

    Listed drug product patent expiration.

    in 8 yr 4 mo

  14. Patent 12178918 expires

    Listed drug product patent expiration.

    in 8 yr 4 mo

  15. Patent 12178919 expires

    Listed drug product patent expiration.

    in 8 yr 4 mo

  16. Patent 12274793 expires

    Listed drug product patent expiration.

    in 8 yr 4 mo

  17. Patent 12303605 expires

    Listed drug product patent expiration.

    in 8 yr 4 mo

  18. Patent 12403099 expires

    Listed drug product patent expiration.

    in 8 yr 4 mo

  19. Patent 12491164 expires

    Listed drug product patent expiration.

    in 8 yr 4 mo

  20. Patent 11986449 expires

    Listed method-of-use patent (U-219) expiration.

    in 15 yr 8 mo

  21. Patent 12109185 expires

    Listed method-of-use patent (U-1649) expiration.

    in 15 yr 8 mo

  22. Patent 12109185 expires

    Listed method-of-use patent (U-219) expiration.

    in 15 yr 8 mo

  23. Patent 12109185 expires

    Listed method-of-use patent (U-4004) expiration.

    in 15 yr 8 mo

  24. Patent 12109185 expires

    Listed method-of-use patent (U-4005) expiration.

    in 15 yr 8 mo

  25. Patent 12194150 expires

    Listed method-of-use patent (U-219) expiration.

    in 15 yr 8 mo

  26. Patent 12201596 expires

    Listed method-of-use patent (U-1649) expiration.

    in 15 yr 8 mo

  27. Patent 12201596 expires

    Listed method-of-use patent (U-4004) expiration.

    in 15 yr 8 mo

  28. Patent 12201596 expires

    Listed method-of-use patent (U-4005) expiration.

    in 15 yr 8 mo

  29. Patent 12263148 expires

    Listed method-of-use patent (U-1649) expiration.

    in 15 yr 8 mo

  30. Patent 12263148 expires

    Listed method-of-use patent (U-4004) expiration.

    in 15 yr 8 mo

  31. Patent 12263148 expires

    Listed method-of-use patent (U-219) expiration.

    in 15 yr 8 mo

  32. Patent 12263148 expires

    Listed method-of-use patent (U-4005) expiration.

    in 15 yr 8 mo

  33. Patent 12263149 expires

    Listed method-of-use patent (U-1649) expiration.

    in 15 yr 8 mo

  34. Patent 12263149 expires

    Listed method-of-use patent (U-219) expiration.

    in 15 yr 8 mo

  35. Patent 12263149 expires

    Listed method-of-use patent (U-4004) expiration.

    in 15 yr 8 mo

  36. Patent 12263149 expires

    Listed method-of-use patent (U-4005) expiration.

    in 15 yr 8 mo

  37. Patent 12295931 expires

    Listed method-of-use patent (U-1649) expiration.

    in 15 yr 8 mo

  38. Patent 12295931 expires

    Listed method-of-use patent (U-4005) expiration.

    in 15 yr 8 mo

  39. Patent 12295931 expires

    Listed method-of-use patent (U-4004) expiration.

    in 15 yr 8 mo

  40. Patent 12295931 expires

    Listed method-of-use patent (U-219) expiration.

    in 15 yr 8 mo

  41. Patent 12303481 expires

    Listed method-of-use patent (U-1649) expiration.

    in 15 yr 8 mo

  42. Patent 12303481 expires

    Listed method-of-use patent (U-219) expiration.

    in 15 yr 8 mo

  43. Patent 12303481 expires

    Listed method-of-use patent (U-4004) expiration.

    in 15 yr 8 mo

  44. Patent 12303481 expires

    Listed method-of-use patent (U-4005) expiration.

    in 15 yr 8 mo

  45. Patent 12303482 expires

    Listed method-of-use patent (U-1649) expiration.

    in 15 yr 8 mo

  46. Patent 12303482 expires

    Listed method-of-use patent (U-4005) expiration.

    in 15 yr 8 mo

  47. Patent 12303482 expires

    Listed method-of-use patent (U-4004) expiration.

    in 15 yr 8 mo

  48. Patent 12303482 expires

    Listed method-of-use patent (U-219) expiration.

    in 15 yr 8 mo

  49. Patent 12370163 expires

    Listed method-of-use patent (U-1649) expiration.

    in 15 yr 8 mo

  50. Patent 12370163 expires

    Listed method-of-use patent (U-219) expiration.

    in 15 yr 8 mo

  51. Patent 12370163 expires

    Listed method-of-use patent (U-4004) expiration.

    in 15 yr 8 mo

  52. Patent 12370163 expires

    Listed method-of-use patent (U-4005) expiration.

    in 15 yr 8 mo

  53. Patent 12447139 expires

    Listed method-of-use patent (U-1649) expiration.

    in 15 yr 8 mo

  54. Patent 12447139 expires

    Listed method-of-use patent (U-219) expiration.

    in 15 yr 8 mo

  55. Patent 12447139 expires

    Listed method-of-use patent (U-4004) expiration.

    in 15 yr 8 mo

  56. Patent 12447139 expires

    Listed method-of-use patent (U-4005) expiration.

    in 15 yr 8 mo

  57. Patent 12453710 expires

    Listed method-of-use patent (U-4005) expiration.

    in 15 yr 8 mo

  58. Patent 12453710 expires

    Listed method-of-use patent (U-4004) expiration.

    in 15 yr 8 mo

  59. Patent 12453710 expires

    Listed method-of-use patent (U-219) expiration.

    in 15 yr 8 mo

  60. Patent 12453710 expires

    Listed method-of-use patent (U-1649) expiration.

    in 15 yr 8 mo

  61. Patent 12458616 expires

    Listed method-of-use patent (U-1649) expiration.

    in 15 yr 8 mo

  62. Patent 12458616 expires

    Listed method-of-use patent (U-4005) expiration.

    in 15 yr 8 mo

  63. Patent 12458616 expires

    Listed method-of-use patent (U-4004) expiration.

    in 15 yr 8 mo

  64. Patent 12458616 expires

    Listed method-of-use patent (U-219) expiration.

    in 15 yr 8 mo

Patent & exclusivity timeline

Protection horizon
202620282030203220342036203820402042TodayExclusivity NP: 2027-08-07Exclusivity NPPatent 10098845: 2034-10-07Patent 10098845Patent 10292935: 2034-10-07Patent 10292935Patent 10688058: 2034-10-07Patent 10688058Patent 10973769: 2034-10-07Patent 10973769Patent 10987313: 2034-10-07Patent 10987313Patent 11357733: 2034-10-07Patent 11357733Patent 11622941: 2034-10-07Patent 11622941Patent 11666538: 2034-10-07Patent 11666538Patent 12064521: 2034-10-07Patent 12064521Patent 12128141: 2034-10-07Patent 12128141Patent 12178918: 2034-10-07Patent 12178918Patent 12178919: 2034-10-07Patent 12178919Patent 12274793: 2034-10-07Patent 12274793Patent 12303605: 2034-10-07Patent 12303605Patent 12403099: 2034-10-07Patent 12403099Patent 12491164: 2034-10-07Patent 12491164Patent 11986449: 2041-12-21Patent 11986449Patent 12109185: 2041-12-21Patent 12109185Patent 12109185: 2041-12-21Patent 12109185Patent 12109185: 2041-12-21Patent 12109185Patent 12109185: 2041-12-21Patent 12109185Patent 12194150: 2041-12-21Patent 12194150Patent 12201596: 2041-12-21Patent 12201596Patent 12201596: 2041-12-21Patent 12201596Patent 12201596: 2041-12-21Patent 12201596Patent 12263148: 2041-12-21Patent 12263148Patent 12263148: 2041-12-21Patent 12263148Patent 12263148: 2041-12-21Patent 12263148Patent 12263148: 2041-12-21Patent 12263148Patent 12263149: 2041-12-21Patent 12263149Patent 12263149: 2041-12-21Patent 12263149Patent 12263149: 2041-12-21Patent 12263149Patent 12263149: 2041-12-21Patent 12263149Patent 12295931: 2041-12-21Patent 12295931Patent 12295931: 2041-12-21Patent 12295931Patent 12295931: 2041-12-21Patent 12295931Patent 12295931: 2041-12-21Patent 12295931Patent 12303481: 2041-12-21Patent 12303481Patent 12303481: 2041-12-21Patent 12303481Patent 12303481: 2041-12-21Patent 12303481Patent 12303481: 2041-12-21Patent 12303481Patent 12303482: 2041-12-21Patent 12303482Patent 12303482: 2041-12-21Patent 12303482Patent 12303482: 2041-12-21Patent 12303482Patent 12303482: 2041-12-21Patent 12303482Patent 12370163: 2041-12-21Patent 12370163Patent 12370163: 2041-12-21Patent 12370163Patent 12370163: 2041-12-21Patent 12370163Patent 12370163: 2041-12-21Patent 12370163Patent 12447139: 2041-12-21Patent 12447139Patent 12447139: 2041-12-21Patent 12447139Patent 12447139: 2041-12-21Patent 12447139Patent 12447139: 2041-12-21Patent 12447139Patent 12453710: 2041-12-21Patent 12453710Patent 12453710: 2041-12-21Patent 12453710Patent 12453710: 2041-12-21Patent 12453710Patent 12453710: 2041-12-21Patent 12453710Patent 12458616: 2041-12-21Patent 12458616Patent 12458616: 2041-12-21Patent 12458616Patent 12458616: 2041-12-21Patent 12458616Patent 12458616: 2041-12-21Patent 12458616
Patent expiryExclusivity endToday

Pharmaceutical detail

FDA product record

Active ingredient

CARBIDOPA; LEVODOPA

Strength

35MG;140MG

Dosage form

CAPSULE, EXTENDED RELEASE

Route

ORAL

TE code

Not listed

Application

NDA 217186

Product number

001

Marketing status

Prescription

Reference listed drug (RLD)

Yes

Reference standard (RS)

No

Marketing exclusivity

Hatch-Waxman
  • NPNew product exclusivity (3 years)

    in 1 yr 1 mo

Listed patents

Orange Book patent file
Patents listed in the FDA Orange Book for this product, with expiration date and patent type.
PatentExpiresInType
10098845in 8 yr 4 mo
ProductU-219
10292935in 8 yr 4 mo
ProductU-219
10688058in 8 yr 4 mo
ProductU-219
10973769in 8 yr 4 mo
ProductU-219
10987313in 8 yr 4 mo
ProductU-219
11357733in 8 yr 4 mo
Product
11622941in 8 yr 4 mo
Product
11666538in 8 yr 4 mo
ProductU-219
12064521in 8 yr 4 mo
Product
12128141in 8 yr 4 mo
ProductU-219
12178918in 8 yr 4 mo
Product
12178919in 8 yr 4 mo
ProductU-219
12274793in 8 yr 4 mo
Product
12303605in 8 yr 4 mo
Product
12403099in 8 yr 4 mo
Product
12491164in 8 yr 4 mo
Product
11986449in 15 yr 8 mo
U-219
12109185in 15 yr 8 mo
U-1649
12109185in 15 yr 8 mo
U-219
12109185in 15 yr 8 mo
U-4004
12109185in 15 yr 8 mo
U-4005
12194150in 15 yr 8 mo
U-219
12201596in 15 yr 8 mo
U-1649
12201596in 15 yr 8 mo
U-4004
12201596in 15 yr 8 mo
U-4005
12263148in 15 yr 8 mo
U-1649
12263148in 15 yr 8 mo
U-4004
12263148in 15 yr 8 mo
U-219
12263148in 15 yr 8 mo
U-4005
12263149in 15 yr 8 mo
U-1649
12263149in 15 yr 8 mo
U-219
12263149in 15 yr 8 mo
U-4004
12263149in 15 yr 8 mo
U-4005
12295931in 15 yr 8 mo
U-1649
12295931in 15 yr 8 mo
U-4005
12295931in 15 yr 8 mo
U-4004
12295931in 15 yr 8 mo
U-219
12303481in 15 yr 8 mo
U-1649
12303481in 15 yr 8 mo
U-219
12303481in 15 yr 8 mo
U-4004
12303481in 15 yr 8 mo
U-4005
12303482in 15 yr 8 mo
U-1649
12303482in 15 yr 8 mo
U-4005
12303482in 15 yr 8 mo
U-4004
12303482in 15 yr 8 mo
U-219
12370163in 15 yr 8 mo
U-1649
12370163in 15 yr 8 mo
U-219
12370163in 15 yr 8 mo
U-4004
12370163in 15 yr 8 mo
U-4005
12447139in 15 yr 8 mo
U-1649
12447139in 15 yr 8 mo
U-219
12447139in 15 yr 8 mo
U-4004
12447139in 15 yr 8 mo
U-4005
12453710in 15 yr 8 mo
U-4005
12453710in 15 yr 8 mo
U-4004
12453710in 15 yr 8 mo
U-219
12453710in 15 yr 8 mo
U-1649
12458616in 15 yr 8 mo
U-1649
12458616in 15 yr 8 mo
U-4005
12458616in 15 yr 8 mo
U-4004
12458616in 15 yr 8 mo
U-219

Active-ingredient family

Brand + generics

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.

Crexont: 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 217186 is shown on this page. Interpret patents, exclusivity, availability, and therapeutic equivalence using the limitations above.

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