Drybench Patent.
BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE, NDA 204242
The patents and exclusivities FDA's Orange Book lists for NDA 204242 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.
Listed protection
Listed dates run from 3 Dec 2027 to 18 Sep 2032, each by its own rule; no one date stands for this product.
- Earliest listed date
- 3 Dec 2027US 8,658,198, product and use patentRule R1 · Products 001, 002, 003, 004, 005, 006 · patent.txt lines 4,376, 4,386, 4,395, 4,404, 4,413, 4,420
- Latest listed date
- 18 Sep 2032US 9,439,900, product patentRule R1 · Products 001, 002, 003, 004, 005 · patent.txt lines 4,379, 4,389, 4,398, 4,407, 4,416
- Latest substance patent
- None listed
- Latest listed patent
- 18 Sep 2032US 9,439,900, product patentRule R1 · Products 001, 002, 003, 004, 005 · patent.txt lines 4,379, 4,389, 4,398, 4,407, 4,416
- Latest exclusivity
- None listed
27 use-code patents, blocking the coded use only
Products
Each product number FDA lists under NDA 204242, as listed. The sections below name products by these numbers.
Product 001 · ZUBSOLV
- Dosage form; route
- TABLET;SUBLINGUAL
- Strength
- EQ 1.4MG BASE;EQ 0.36MG BASE
- Approval date as listed
- 3 Jul 2013
- Type as listed
- RX
- Applicant as listed
- EDENBRIDGE PHARMACEUTICALS LLC DBA DEXCEL PHARMA USA
Product 002 · ZUBSOLV
- Dosage form; route
- TABLET;SUBLINGUAL
- Strength
- EQ 5.7MG BASE;EQ 1.4MG BASE
- Approval date as listed
- 3 Jul 2013
- Type as listed
- RX
- Applicant as listed
- EDENBRIDGE PHARMACEUTICALS LLC DBA DEXCEL PHARMA USA
Product 003 · ZUBSOLV
- Dosage form; route
- TABLET;SUBLINGUAL
- Strength
- EQ 8.6MG BASE;EQ 2.1MG BASE
- Approval date as listed
- 11 Dec 2014
- Type as listed
- RX
- Applicant as listed
- EDENBRIDGE PHARMACEUTICALS LLC DBA DEXCEL PHARMA USA
Product 004 · ZUBSOLV
- Dosage form; route
- TABLET;SUBLINGUAL
- Strength
- EQ 11.4MG BASE;EQ 2.9MG BASE
- Approval date as listed
- 11 Dec 2014
- Type as listed
- RX
- Applicant as listed
- EDENBRIDGE PHARMACEUTICALS LLC DBA DEXCEL PHARMA USA
Product 005 · ZUBSOLV
- Dosage form; route
- TABLET;SUBLINGUAL
- Strength
- EQ 2.9MG BASE;EQ 0.71MG BASE
- Approval date as listed
- 4 Jun 2015
- Type as listed
- RX
- Applicant as listed
- EDENBRIDGE PHARMACEUTICALS LLC DBA DEXCEL PHARMA USA
Product 006 · ZUBSOLV
- Dosage form; route
- TABLET;SUBLINGUAL
- Strength
- EQ 0.7MG BASE;EQ 0.18MG BASE
- Approval date as listed
- 4 Oct 2016
- Type as listed
- RX
- Applicant as listed
- EDENBRIDGE PHARMACEUTICALS LLC DBA DEXCEL PHARMA USA
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.
10 entries from 51 rows as listed; rows merge only where every cell shown is the same, each with its product numbers.
US 8,658,198, product and use patent
patent.txt lines 4,376, 4,386, 4,395, 4,404, 4,413, 4,420- Expiry as listed
- 3 Dec 2027
- Rule
- R1
- Flags
- product · use code U-1494
- Product numbers
- 001, 002, 003, 004, 005, 006
US 8,470,361, product and use patent
patent.txt lines 4,375, 4,385, 4,394, 4,403, 4,412, 4,419- Expiry as listed
- 22 May 2030
- Rule
- R1
- Flags
- product · use code U-1425
- Product numbers
- 001, 002, 003, 004, 005, 006
US 10,874,661, product patent
patent.txt line 4,380- Expiry as listed
- 18 Sep 2032
- Rule
- R1
- Flags
- product
- Product numbers
- 002
US 10,946,010, product patent
patent.txt lines 4,372, 4,381, 4,390, 4,399, 4,408, 4,417- Expiry as listed
- 18 Sep 2032
- Rule
- R1
- Flags
- product
- Product numbers
- 001, 002, 003, 004, 005, 006
US 11,020,387, product and use patent
patent.txt lines 4,382, 4,391, 4,400, 4,409- Expiry as listed
- 18 Sep 2032
- Rule
- R1
- Flags
- product · use code U-3131
- Product numbers
- 002, 003, 004, 005
US 11,020,388, product and use patent
patent.txt lines 4,373, 4,383, 4,392, 4,401, 4,410, 4,418- Expiry as listed
- 18 Sep 2032
- Rule
- R1
- Flags
- product · use code U-3131
- Product numbers
- 001, 002, 003, 004, 005, 006
US 11,433,066, use patent
patent.txt lines 4,374, 4,384, 4,393, 4,402, 4,411- Expiry as listed
- 18 Sep 2032
- Rule
- R1
- Flags
- use code U-3131
- Product numbers
- 001, 002, 003, 004, 005
US 8,940,330, product patent
patent.txt lines 4,377, 4,387, 4,396, 4,405, 4,414, 4,421- Expiry as listed
- 18 Sep 2032
- Rule
- R1
- Flags
- product
- Product numbers
- 001, 002, 003, 004, 005, 006
US 9,259,421, product patent
patent.txt lines 4,378, 4,388, 4,397, 4,406, 4,415, 4,422- Expiry as listed
- 18 Sep 2032
- Rule
- R1
- Flags
- product
- Product numbers
- 001, 002, 003, 004, 005, 006
US 9,439,900, product patent
patent.txt lines 4,379, 4,389, 4,398, 4,407, 4,416- Expiry as listed
- 18 Sep 2032
- Rule
- R1
- Flags
- product
- Product numbers
- 001, 002, 003, 004, 005
Listed exclusivities
Each exclusivity FDA lists for NDA 204242, 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 204242.
Paragraph IV list rows giving NDA 204242
The rows of FDA's Paragraph IV certifications list as captured on 17 October 2026 whose RLD/NDA cell gives NDA 204242, 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 204242
Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate · Sublingual Tablets · 1.4 mg/0.36 mg and 5.7 mg/1.4 mg
RLD/NDA as listed: Zubsolv 204242- First PIV submission
- 22 Oct 2013
- ANDAs
- 1
- 180-day status
- Extinguished
- Decision posted
- 3 Oct 2024
- First applicant approval
- blank
- First marketing
- blank
- Last qualifying patent expiry (as listed by FDA)
- 22 May 2030
Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate · Sublingual Tablets · 0.7 mg/0.18 mg
RLD/NDA as listed: Zubsolv 204242- First PIV submission
- 4 May 2017
- ANDAs
- 1
- 180-day status
- Extinguished
- Decision posted
- 3 Oct 2024
- First applicant approval
- blank
- First marketing
- blank
- Last qualifying patent expiry (as listed by FDA)
- 18 Sep 2032
Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate · Sublingual Tablets · 2.9 mg/7.1 mg
RLD/NDA as listed: Zubsolv 204242- First PIV submission
- 21 Dec 2015
- ANDAs
- 1
- 180-day status
- Extinguished
- Decision posted
- 3 Oct 2024
- First applicant approval
- blank
- First marketing
- blank
- Last qualifying patent expiry (as listed by FDA)
- 18 Sep 2032
Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate · Sublingual Tablets · 8.6 mg/2.1 mg and 11.4 mg/2.9 mg
RLD/NDA as listed: Zubsolv 204242- First PIV submission
- 24 Jul 2015
- ANDAs
- 1
- 180-day status
- Extinguished
- Decision posted
- 3 Oct 2024
- First applicant approval
- blank
- First marketing
- blank
- Last qualifying patent expiry (as listed by FDA)
- 18 Sep 2032
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