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CYCLOSPORINE, NDA 050790

The patents and exclusivities FDA's Orange Book lists for NDA 050790 as captured on 14 October 2026, each date named by its rule and its rows, and the rows of FDA's Paragraph IV list that give this NDA's number, as captured on 17 October 2026. Listed protection is a range of dates, never one date.

FDA capture · review pending. Each row is shown as captured from FDA's Orange Book files and Paragraph IV list. Dates are FDA's own; spreadsheet day numbers are shown as dates, and a cell that cannot be read as one date is shown as written and left out of the range. Where FDA lists a *PED row without flags, its flags are read from the base row and marked so. A Paragraph IV row is placed here only by the number in its RLD/NDA cell; nothing is joined by name. How this page reads FDA's files has not been independently reviewed by a regulatory-affairs reviewer.

Orange Book captured
14 October 2026
Paragraph IV list captured
17 October 2026
Last checked
30 October 2026
Data-branch commit
dadcab56563716abea6c5e31a5e1970080c778ef

Listed protection is a range of the dates FDA lists, not a forecast of market entry, and not legal, regulatory or investment advice.

Dates as listed in FDA's Orange Book capture of 14 October 2026. This page does not say whether a date has passed; compare it with today's date and FDA's current Orange Book. This page shows only what the capture of 14 October 2026 lists. It does not show patents or exclusivities listed before and since removed.

Open in the appCYCLOSPORINE in the molecule app

Listed protection

Listed dates run from 25 Feb 2031 to 11 May 2034, each by its own rule; no one date stands for this product.

Earliest listed date
25 Feb 2031US 8,292,129, product patentRule R1 · Product 002 · patent.txt line 2,140
Latest listed date
11 May 2034US 9,669,974, product patentRule R1 · Product 002 · patent.txt line 2,142
Latest substance patent
None listed
Latest listed patent
11 May 2034US 9,669,974, product patentRule R1 · Product 002 · patent.txt line 2,142
Latest exclusivity
None listed

4 patents with a delist request, kept in the table

Products

Each product number FDA lists under NDA 050790, as listed. The sections below name products by these numbers.

  • Product 001 · RESTASIS

    Dosage form; route
    EMULSION;OPHTHALMIC
    Strength
    0.05%
    Approval date as listed
    23 Dec 2002
    Type as listed
    RX
    Applicant as listed
    ABBVIE INC

  • Product 002 · RESTASIS MULTIDOSE

    Dosage form; route
    EMULSION;OPHTHALMIC
    Strength
    0.05%
    Approval date as listed
    27 Oct 2016
    Type as listed
    RX
    Applicant as listed
    ABBVIE INC

Listed patents

Every patent the FDA lists for this product, as the application holder submitted it, with its flags. The FDA does not verify listings.

4 entries from 4 rows as listed; rows merge only where every cell shown is the same, each with its product numbers.

  • US 8,292,129, product patent

    patent.txt line 2,140
    Expiry as listed
    25 Feb 2031
    Rule
    R1
    Flags
    product · delist requested
    Product numbers
    002

  • US 8,561,859, product patent

    patent.txt line 2,141
    Expiry as listed
    16 Apr 2032
    Rule
    R1
    Flags
    product · delist requested
    Product numbers
    002

  • US 9,676,525, product patent

    patent.txt line 2,143
    Expiry as listed
    7 Feb 2034
    Rule
    R1
    Flags
    product · delist requested
    Product numbers
    002

  • US 9,669,974, product patent

    patent.txt line 2,142
    Expiry as listed
    11 May 2034
    Rule
    R1
    Flags
    product · delist requested
    Product numbers
    002

Listed exclusivities

Each exclusivity FDA lists for NDA 050790, with its code, FDA's definition of the code where the store's code list gives one, and its date as listed.

The Orange Book capture of 14 October 2026 lists no exclusivity for NDA 050790.

Paragraph IV list rows giving NDA 050790

The rows of FDA's Paragraph IV certifications list as captured on 17 October 2026 whose RLD/NDA cell gives NDA 050790, each cell as listed.

FDA's Paragraph IV list names no patent number, so it does not say which of the patents on this page an applicant certified against.

The list gives the last qualifying patent's expiry without pediatric exclusivity; in the app's Patents view, the Orange Book lists any *PED period as a separate row with its own date. The two dates describe different things. A blank cell is one FDA left blank in its list. Dates are FDA's own; the last qualifying patent expiry is not recomputed from the Orange Book.

Rows whose RLD/NDA cell we could not read as exactly one NDA number are kept apart on the list page; some may concern this product.

Rows on FDA's Paragraph IV list whose RLD/NDA cell gives NDA 050790

  • Cyclosporine · Ophthalmic Emulsion · 5.0000000000000001E-4

    RLD/NDA as listed: Restasis 50790
    First PIV submission
    13 Jan 2014
    ANDAs
    1
    180-day status
    Extinguished
    Decision posted
    8 Feb 2022
    First applicant approval
    blank
    First marketing
    blank
    Last qualifying patent expiry (as listed by FDA)
    17 May 2014

  • Cyclosporine · Ophthalmic Emulsion · 5.0000000000000001E-4

    RLD/NDA as listed: Restasis Multidose 50790
    First PIV submission
    29 Jan 2020
    ANDAs
    1
    180-day status
    blank
    Decision posted
    blank
    First applicant approval
    blank
    First marketing
    blank
    Last qualifying patent expiry (as listed by FDA)
    11 May 2034

Notes from the trace

  • R6 tentative approvals: not in the Orange Book data files as captured; the Drugs@FDA join is a later ruling.

Patents vs FDA exclusivityHow to read the Orange Book data filesParagraph IV certificationWhat changed, by week