Skip to content

Drybench Patent.

TIGECYCLINE, NDA 211158

The patents and exclusivities FDA's Orange Book lists for NDA 211158 as captured on 14 October 2026, each date named by its rule and its rows, and any rows of FDA's Paragraph IV list captured on 17 October 2026 that give this NDA's number. 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 appTIGECYCLINE in the molecule app

Listed protection

Listed dates run from 7 Apr 2033 to 7 Apr 2033, each by its own rule; no one date stands for this product.

Earliest listed date
7 Apr 2033US 9,855,335, product patentRule R1 · Product 001
Source lines

patent.txt line 12,506

Latest listed date
7 Apr 2033US 9,855,335, product patentRule R1 · Product 001
Source lines

patent.txt line 12,506

Latest substance patent
None listed
Latest listed patent
7 Apr 2033US 9,855,335, product patentRule R1 · Product 001
Source lines

patent.txt line 12,506

Latest exclusivity
None listed

Listed dates of other NDAs in the same years:2033

Products

Each product number FDA lists under NDA 211158, as listed. The sections below name products by these numbers.

  • Product 001 · TIGECYCLINE

    Dosage form; route
    POWDER;INTRAVENOUS
    Strength
    50MG/VIAL
    Approval date as listed
    2 Aug 2018
    Type as listed
    RX
    Applicant as listed
    AMNEAL PHARMACEUTICALS LLC

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.

1 entry from 1 row as listed; rows merge only where every cell shown is the same, each with its product numbers.

  • US 9,855,335, product patent

    patent.txt line 12,506
    Expiry as listed
    7 Apr 2033
    Rule
    R1
    Flags
    product
    Product numbers
    001

Listed exclusivities

Each exclusivity FDA lists for NDA 211158, 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 211158.

Paragraph IV list rows giving NDA 211158

The rows of FDA's Paragraph IV certifications list as captured on 17 October 2026 whose RLD/NDA cell gives NDA 211158, each cell as listed.

Rows with no NDA number this page can match are kept apart on the list page; some may concern this product.

No row of the Paragraph IV list captured on 17 October 2026 gives NDA 211158 in its RLD/NDA cell. This does not mean no certification was submitted or that no application challenges a patent listed here.

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