Anktiva 400 MCG per 0.4 ML Intravesical Solution

RxCUI
2682691
RxNorm name
Anktiva 400 MCG per 0.4 ML Intravesical Solution
Display name
Anktiva 400 MCG per 0.4 ML Intravesical Solution
Full name
Anktiva 400 MCG per 0.4 ML Intravesical Solution
Term type
SY
Status
DailyMed mapping
Updated
2026-06-04 23:39:26

Purple Book Biologic Products#

BLA, Proprietary name, Proper name table
BLAProprietary nameProper nameLicense typeStatusLatest source
761336Anktivanogapendekin alfa inbakicept-pmln351(a)Rx2026-08-01

RxNav Current And Historical NDCs#

RxNav current and historical NDC rows page 1 of 1 · 0 matching rows.

No records found.

UNII Substances#

UNII substance links page 1 of 1 · 0 matching rows.

No records found.

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ANKTIVANOGAPENDEKIN ALFA INBAKICEPT-PMLNAltor BioScience, LLC, an indirect wholly-owned subsidiary of ImmunityBio, Inc.eae31db8-3e7a-d9e0-708d-74419d1b50ff2025-06-24Warnings, Adverse reactionsExact identifier
rxcui: 2682691

DailyMed RxNorm Mappings#

unique DailyMed labels mapped to this RxNorm concept page 1 of 1 · 1 matching rows.

Set ID, RxNorm mappings, Terms table
Set IDRxNorm mappingsTermsSPL versionLabelEffective
eae31db8-3e7a-d9e0-708d-74419d1b50ffAnktiva 400 MCG in 0.4 ML Intravesical Solution [PSN] · 0.4 ML nogapendekin alfa inbakicept-pmln 1 MG/ML Intravesical Solution [Anktiva] [SBD] · 0.4 ML Anktiva 1 MG/ML Intravesical Solution [SY] · Anktiva 400 MCG per 0.4 ML Intravesical Solution [SY]49These highlights do not include all the information needed to use ANKTIVA safely and effectively. See full prescribing information for ANKTIVA. ANKTIVA® (nogapendekin alfa inbakicept-pmln) solution, for intravesical use Initial U.S. Approval: 202420250624