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Drybench Patent.

EMPAGLIFLOZIN; LINAGLIPTIN, NDA 206073

The patents and exclusivities FDA's Orange Book lists for NDA 206073 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.

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Listed protection

Listed dates run from 26 Nov 2025 to 8 Dec 2037, each by its own rule; no one date stands for this product.

Earliest listed date
26 Nov 2025US 8,883,805, product patentRule R1 · Products 001, 002 · patent.txt lines 6,202, 6,234
Latest listed date
8 Dec 2037US 12,364,700 with pediatric exclusivity, as listedRule R2 · Products 001, 002 · patent.txt lines 6,185, 6,217
Latest substance patent
1 Feb 2029US 7,579,449 with pediatric exclusivity, as listedRule R2 · Products 001, 002 · patent.txt lines 6,193, 6,225
Latest listed patent
8 Dec 2037US 12,364,700 with pediatric exclusivity, as listedRule R2 · Products 001, 002 · patent.txt lines 6,185, 6,217
Latest exclusivity
None listed

4 patents with a delist request, kept in the table · 30 use-code patents, blocking the coded use only

Products

Each product number FDA lists under NDA 206073, as listed. The sections below name products by these numbers.

  • Product 001 · GLYXAMBI

    Dosage form; route
    TABLET;ORAL
    Strength
    10MG;5MG
    Approval date as listed
    30 Jan 2015
    Type as listed
    RX
    Applicant as listed
    BOEHRINGER INGELHEIM
  • Product 002 · GLYXAMBI

    Dosage form; route
    TABLET;ORAL
    Strength
    25MG;5MG
    Approval date as listed
    30 Jan 2015
    Type as listed
    RX
    Applicant as listed
    BOEHRINGER INGELHEIM

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.

32 entries from 64 rows as listed; rows merge only where every cell shown is the same, each with its product numbers.

  • US 8,883,805, product patent

    patent.txt lines 6,202, 6,234
    Expiry as listed
    26 Nov 2025
    Rule
    R1
    Flags
    product
    Product numbers
    001, 002
  • US 8,883,805 with pediatric exclusivity, as listed

    patent.txt lines 6,201, 6,233
    Expiry as listed
    26 May 2026
    Rule
    R2
    Flags
    product · pediatric, as listed by FDA (from the base row)
    Product numbers
    001, 002
  • US 7,713,938, substance and product patent

    patent.txt lines 6,196, 6,228
    Expiry as listed
    15 Apr 2027
    Rule
    R1
    Flags
    substance · product
    Product numbers
    001, 002
  • US 11,033,552, product patent

    patent.txt lines 6,176, 6,208
    Expiry as listed
    4 May 2027
    Rule
    R1
    Flags
    product
    Product numbers
    001, 002
  • US 12,178,819, product patent

    patent.txt lines 6,184, 6,216
    Expiry as listed
    4 May 2027
    Rule
    R1
    Flags
    product
    Product numbers
    001, 002
  • US 8,673,927, use patent

    patent.txt lines 6,200, 6,232
    Expiry as listed
    4 May 2027
    Rule
    R1
    Flags
    use code U-1652 · delist requested
    Product numbers
    001, 002
  • US 9,173,859, product and use patent

    patent.txt lines 6,203, 6,235
    Expiry as listed
    4 May 2027
    Rule
    R1
    Flags
    product · use code U-1772 · delist requested
    Product numbers
    001, 002
  • US 7,713,938 with pediatric exclusivity, as listed

    patent.txt lines 6,195, 6,227
    Expiry as listed
    15 Oct 2027
    Rule
    R2
    Flags
    substance · product · pediatric, as listed by FDA (from the base row)
    Product numbers
    001, 002
  • US 11,033,552 with pediatric exclusivity, as listed

    patent.txt lines 6,175, 6,207
    Expiry as listed
    4 Nov 2027
    Rule
    R2
    Flags
    product · pediatric, as listed by FDA (from the base row)
    Product numbers
    001, 002
  • US 8,673,927 with pediatric exclusivity, as listed

    patent.txt lines 6,199, 6,231
    Expiry as listed
    4 Nov 2027
    Rule
    R2
    Flags
    pediatric, as listed by FDA (from the base row)
    Product numbers
    001, 002
  • US 7,579,449, substance patent

    patent.txt lines 6,194, 6,226
    Expiry as listed
    1 Aug 2028
    Rule
    R1
    Flags
    substance
    Product numbers
    001, 002
  • US 7,579,449 with pediatric exclusivity, as listed

    patent.txt lines 6,193, 6,225
    Expiry as listed
    1 Feb 2029
    Rule
    R2
    Flags
    substance · pediatric, as listed by FDA (from the base row)
    Product numbers
    001, 002
  • US 8,551,957, product and use patent

    patent.txt lines 6,198, 6,230
    Expiry as listed
    14 Oct 2029
    Rule
    R1
    Flags
    product · use code U-1651
    Product numbers
    001, 002
  • US 12,115,179, use patent

    patent.txt lines 6,183, 6,215
    Expiry as listed
    11 Feb 2030
    Rule
    R1
    Flags
    use code U-4023
    Product numbers
    001, 002
  • US 8,551,957 with pediatric exclusivity, as listed

    patent.txt lines 6,197, 6,229
    Expiry as listed
    14 Apr 2030
    Rule
    R2
    Flags
    product · pediatric, as listed by FDA (from the base row)
    Product numbers
    001, 002
  • US 12,115,179 with pediatric exclusivity, as listed

    patent.txt lines 6,182, 6,214
    Expiry as listed
    11 Aug 2030
    Rule
    R2
    Flags
    pediatric, as listed by FDA (from the base row)
    Product numbers
    001, 002
  • US 10,258,637, use patent

    patent.txt lines 6,174, 6,206
    Expiry as listed
    3 Apr 2034
    Rule
    R1
    Flags
    use code U-2290
    Product numbers
    001, 002
  • US 11,090,323, use patent

    patent.txt lines 6,178, 6,210
    Expiry as listed
    3 Apr 2034
    Rule
    R1
    Flags
    use code U-3191
    Product numbers
    001, 002
  • US 11,833,166, use patent

    patent.txt lines 6,180, 6,212
    Expiry as listed
    3 Apr 2034
    Rule
    R1
    Flags
    use code U-3776
    Product numbers
    001, 002
  • US 11,833,166, use patent

    patent.txt lines 6,181, 6,213
    Expiry as listed
    3 Apr 2034
    Rule
    R1
    Flags
    use code U-3777
    Product numbers
    001, 002
  • US 12,433,906, use patent

    patent.txt lines 6,188, 6,220
    Expiry as listed
    3 Apr 2034
    Rule
    R1
    Flags
    use code U-4293
    Product numbers
    001, 002
  • US 12,433,906, use patent

    patent.txt lines 6,189, 6,221
    Expiry as listed
    3 Apr 2034
    Rule
    R1
    Flags
    use code U-4294
    Product numbers
    001, 002
  • US 12,433,906, use patent

    patent.txt lines 6,190, 6,222
    Expiry as listed
    3 Apr 2034
    Rule
    R1
    Flags
    use code U-4295
    Product numbers
    001, 002
  • US 12,433,906, use patent

    patent.txt lines 6,191, 6,223
    Expiry as listed
    3 Apr 2034
    Rule
    R1
    Flags
    use code U-4296
    Product numbers
    001, 002
  • US 12,433,906, use patent

    patent.txt lines 6,192, 6,224
    Expiry as listed
    3 Apr 2034
    Rule
    R1
    Flags
    use code U-4304
    Product numbers
    001, 002
  • US 9,949,998, use patent

    patent.txt lines 6,204, 6,236
    Expiry as listed
    11 Jun 2034
    Rule
    R1
    Flags
    use code U-2290
    Product numbers
    001, 002
  • US 10,258,637 with pediatric exclusivity, as listed

    patent.txt lines 6,173, 6,205
    Expiry as listed
    3 Oct 2034
    Rule
    R2
    Flags
    pediatric, as listed by FDA (from the base row)
    Product numbers
    001, 002
  • US 11,090,323 with pediatric exclusivity, as listed

    patent.txt lines 6,177, 6,209
    Expiry as listed
    3 Oct 2034
    Rule
    R2
    Flags
    pediatric, as listed by FDA (from the base row)
    Product numbers
    001, 002
  • US 11,833,166 with pediatric exclusivity, as listed

    patent.txt lines 6,179, 6,211
    Expiry as listed
    3 Oct 2034
    Rule
    R2
    Flags
    pediatric, as listed by FDA (from the base row)
    Product numbers
    001, 002
  • US 12,433,906 with pediatric exclusivity, as listed

    patent.txt lines 6,187, 6,219
    Expiry as listed
    3 Oct 2034
    Rule
    R2
    Flags
    pediatric, as listed by FDA (from the base row)
    Product numbers
    001, 002
  • US 12,364,700, use patent

    patent.txt lines 6,186, 6,218
    Expiry as listed
    8 Jun 2037
    Rule
    R1
    Flags
    use code U-4224
    Product numbers
    001, 002
  • US 12,364,700 with pediatric exclusivity, as listed

    patent.txt lines 6,185, 6,217
    Expiry as listed
    8 Dec 2037
    Rule
    R2
    Flags
    pediatric, as listed by FDA (from the base row)
    Product numbers
    001, 002

Listed exclusivities

Each exclusivity FDA lists for NDA 206073, 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 206073.

Paragraph IV list rows giving NDA 206073

The rows of FDA's Paragraph IV certifications list as captured on 17 October 2026 whose RLD/NDA cell gives NDA 206073, 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 206073

  • Empagliflozin and Linagliptin · Tablets · 10 mg/5 mg and 25 mg/5 mg

    RLD/NDA as listed: Glyxambi 206073
    First PIV submission
    1 Aug 2018
    ANDAs
    9
    180-day status
    blank
    Decision posted
    blank
    First applicant approval
    blank
    First marketing
    blank
    Last qualifying patent expiry (as listed by FDA)
    11 Jun 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