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RIVFLOZA (NEDOSIRAN SODIUM) | LOERadar
Viewing data from:
Latest
2026-07-01
2026-06-01
2026-05-01
2026-04-01
2026-03-28
2026-02-17
2026-02-10
2025-12-14
2025-02-26
2025-01-25
2024-11-08
2023-07-23
2023-06-15
2023-05-13
2023-01-26
2022-11-22
2022-10-28
2022-09-29
2022-07-09
2022-06-29
2022-04-08
2022-03-09
2021-12-28
2021-05-05
2021-03-12
2020-12-22
2020-11-12
2019-12-14
2019-09-15
RIVFLOZA
NDA
NEDOSIRAN SODIUM | N215842 | NOVO NORDISK INC
3 strengths
6 unique patents
4 unique exclusivities
Patents
SEC Intel
Revenue
PTAB
Reexams
Litigation
Petitions
Trials
VA FSS
Approvals
Label
Products
Patent Timeline
6 unique patents, 4 exclusivities by expiration date
All strengths
EQ 80MG BASE/0.5ML (EQ 160MG BASE/ML)
EQ 128MG BASE/0.8ML (EQ 160MG BASE/ML)
EQ 160MG BASE/ML (EQ 160MG BASE/ML)
Active (6)
Today
Exclusivity
2026
2027
2028
2029
2030
2031
2032
2033
2034
2035
2036
2037
2038
2039
Today
10351854
Oct. 9, 2035
10738311
Oct. 9, 2035
11053502
Oct. 29, 2035
11286488
Oct. 12, 2038
11359203
Oct. 9, 2035
11661604
Oct. 12, 2038
NPP
Mar. 27, 2028
NCE
Sep. 29, 2028
ODE-443
Sep. 29, 2030
ODE-531
Mar. 27, 2032
PTAB Proceedings
No IPR/PGR/CBM challenges found at the Patent Trial and Appeal Board
Hatch-Waxman Litigation
No ANDA patent litigation cases (NOS 835) matched from PACER
Citizen Petitions
No FDA citizen petitions matched from Regulations.gov
Products (3)
Sort:
Name
↑
Applicant
Strength
Approval
#001 — EQ 80MG BASE/0.5ML (EQ 160MG BASE/ML)
RLD
6 patents
4 exclusivities
▴
SOLUTION;INJECTION | Approved: Sep 29, 2023
Patents (6)
· 4 use codes
Patent #
Expiration
PED
Drug Substance
Drug Product
Use Code
Delist
10351854
Oct 9, 2035
—
Yes
Yes
—
—
10738311
Oct 9, 2035
—
Yes
Yes
U-3709
METHOD OF TREATING PRIMARY HYPEROXALURIA TYPE 1 (PH1)
—
11053502
Oct 29, 2035
—
Yes
Yes
—
—
11286488
Oct 12, 2038
—
Yes
Yes
U-3709
METHOD OF TREATING PRIMARY HYPEROXALURIA TYPE 1 (PH1)
—
11359203
Oct 9, 2035
—
Yes
Yes
U-3709
METHOD OF TREATING PRIMARY HYPEROXALURIA TYPE 1 (PH1)
—
11661604
Oct 12, 2038
—
Yes
Yes
U-3709
METHOD OF TREATING PRIMARY HYPEROXALURIA TYPE 1 (PH1)
—
Exclusivities (4)
Code
Date
Status
NCE
Sep 29, 2028
Active
NPP
Mar 27, 2028
Active
ODE-443
Sep 29, 2030
Active
ODE-531
Mar 27, 2032
Active
#002 — EQ 128MG BASE/0.8ML (EQ 160MG BASE/ML)
RLD
6 patents
4 exclusivities
▾
SOLUTION;INJECTION | Approved: Sep 29, 2023
#003 — EQ 160MG BASE/ML (EQ 160MG BASE/ML)
RLD
6 patents
4 exclusivities
▾
SOLUTION;INJECTION | Approved: Sep 29, 2023