Drybench Patent.
PALIPERIDONE PALMITATE, NDA 216352
The patents and exclusivities FDA's Orange Book lists for NDA 216352 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.
Listed protection
Listed dates run from 26 Oct 2038 to 24 Sep 2039, each by its own rule; no one date stands for this product.
- Earliest listed date
- 26 Oct 2038US 12,128,049, use patentRule R1 · Products 001, 002, 003, 004, 005, 006
Source lines
patent.txt lines 18,502, 18,506, 18,510, 18,514, 18,518, 18,522
- Latest listed date
- 24 Sep 2039US 11,666,573, use patentRule R1 · Products 001, 002, 003, 004, 005, 006
Source lines
patent.txt lines 18,501, 18,505, 18,509, 18,513, 18,517, 18,521
- Latest substance patent
- None listed
- Latest listed patent
- 24 Sep 2039US 11,666,573, use patentRule R1 · Products 001, 002, 003, 004, 005, 006
Source lines
patent.txt lines 18,501, 18,505, 18,509, 18,513, 18,517, 18,521
- Latest exclusivity
- None listed
Listed dates of other NDAs in the same years:20382039
24 use-code patents, blocking the coded use only
Products
Each product number FDA lists under NDA 216352, as listed. The sections below name products by these numbers.
Product 001 · ERZOFRI
- Dosage form; route
- SUSPENSION, EXTENDED RELEASE;
INTRAMUSCULAR - Strength
- 39MG/0.25ML (39MG/0.25ML)
- Approval date as listed
- 26 Jul 2024
- Type as listed
- RX
- Applicant as listed
- LUYE INNOMIND PHARMA (SHIJIAZHUANG) CO LTD
Product 002 · ERZOFRI
- Dosage form; route
- SUSPENSION, EXTENDED RELEASE;
INTRAMUSCULAR - Strength
- 78MG/0.5ML (78MG/0.5ML)
- Approval date as listed
- 26 Jul 2024
- Type as listed
- RX
- Applicant as listed
- LUYE INNOMIND PHARMA (SHIJIAZHUANG) CO LTD
Product 003 · ERZOFRI
- Dosage form; route
- SUSPENSION, EXTENDED RELEASE;
INTRAMUSCULAR - Strength
- 117MG/0.75ML (117MG/0.75ML)
- Approval date as listed
- 26 Jul 2024
- Type as listed
- RX
- Applicant as listed
- LUYE INNOMIND PHARMA (SHIJIAZHUANG) CO LTD
Product 004 · ERZOFRI
- Dosage form; route
- SUSPENSION, EXTENDED RELEASE;
INTRAMUSCULAR - Strength
- 156MG/ML (156MG/ML)
- Approval date as listed
- 26 Jul 2024
- Type as listed
- RX
- Applicant as listed
- LUYE INNOMIND PHARMA (SHIJIAZHUANG) CO LTD
Product 005 · ERZOFRI
- Dosage form; route
- SUSPENSION, EXTENDED RELEASE;
INTRAMUSCULAR - Strength
- 234MG/1.5ML (156MG/ML)
- Approval date as listed
- 26 Jul 2024
- Type as listed
- RX
- Applicant as listed
- LUYE INNOMIND PHARMA (SHIJIAZHUANG) CO LTD
Product 006 · ERZOFRI
- Dosage form; route
- SUSPENSION, EXTENDED RELEASE;
INTRAMUSCULAR - Strength
- 351MG/2.25ML (156MG/ML)
- Approval date as listed
- 26 Jul 2024
- Type as listed
- RX
- Applicant as listed
- LUYE INNOMIND PHARMA (SHIJIAZHUANG) CO LTD
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 24 rows as listed; rows merge only where every cell shown is the same, each with its product numbers.
US 12,128,049, use patent
patent.txt lines 18,502, 18,506, 18,510, 18,514, 18,518, 18,522- Expiry as listed
- 26 Oct 2038
- Rule
- R1
- Flags
- use code U-3968
- Product numbers
- 001, 002, 003, 004, 005, 006
US 12,128,049, use patent
patent.txt lines 18,503, 18,507, 18,511, 18,515, 18,519, 18,523- Expiry as listed
- 26 Oct 2038
- Rule
- R1
- Flags
- use code U-3969
- Product numbers
- 001, 002, 003, 004, 005, 006
US 11,666,573, use patent
patent.txt lines 18,500, 18,504, 18,508, 18,512, 18,516, 18,520- Expiry as listed
- 24 Sep 2039
- Rule
- R1
- Flags
- use code U-3968
- Product numbers
- 001, 002, 003, 004, 005, 006
US 11,666,573, use patent
patent.txt lines 18,501, 18,505, 18,509, 18,513, 18,517, 18,521- Expiry as listed
- 24 Sep 2039
- Rule
- R1
- Flags
- use code U-3969
- Product numbers
- 001, 002, 003, 004, 005, 006
Listed exclusivities
Each exclusivity FDA lists for NDA 216352, 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 216352.
Paragraph IV list rows giving NDA 216352
The rows of FDA's Paragraph IV certifications list as captured on 17 October 2026 whose RLD/NDA cell gives NDA 216352, 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 216352 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