Fluzone 2025-2026 trivalent vaccine Injectable Suspension

RxCUI
2719216
RxNorm name
Fluzone 2025-2026 trivalent vaccine Injectable Suspension
Display name
Fluzone 2025-2026 trivalent vaccine Injectable Suspension
Full name
Fluzone 2025-2026 trivalent vaccine Injectable Suspension
Term type
SY
Status
DailyMed mapping
Updated
2026-06-04 23:39:00

Purple Book Biologic Products#

BLA, Proprietary name, Proper name table
BLAProprietary nameProper nameLicense typeStatusLatest source
103914Fluzone, Fluzone Hd Quadrivalent, Fluzone High Dose, Fluzone Intradermal, Fluzone QuadrivalentInfluenza Virus Vaccine351(a)Rx2026-06-01

RxNav Current And Historical NDCs#

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UNII Substances#

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No records found.

DailyMed RxNorm Mappings#

Set ID, RxNorm string, TTY table
Set IDRxNorm stringTTYSPL versionLabelEffective
5fe0ce14-bc11-4b43-b002-7efdca0d3003Fluzone 2025-2026 trivalent vaccine Injectable SuspensionSY12These highlights do not include all the information needed to use Fluzone® safely and effectively. See full prescribing information for Fluzone. Fluzone (Influenza Vaccine) injectable suspension, for intramuscular use 2025–2026 Formula Initial U.S. Approval: 198020260325
5fe0ce14-bc11-4b43-b002-7efdca0d3003influenza A virus A/Croatia/10136RV/2023 (H3N2) antigen 0.03 MG/ML / influenza A virus A/Victoria/4897/2022 (H1N1) antigen 0.03 MG/ML / influenza B virus B/Michigan/01/2021 antigen 0.03 MG/ML Injectable Suspension [Fluzone 2025-2026]SBD12These highlights do not include all the information needed to use Fluzone® safely and effectively. See full prescribing information for Fluzone. Fluzone (Influenza Vaccine) injectable suspension, for intramuscular use 2025–2026 Formula Initial U.S. Approval: 198020260325
5fe0ce14-bc11-4b43-b002-7efdca0d3003Fluzone 2025-2026 trivalent vaccine Injectable SuspensionPSN12These highlights do not include all the information needed to use Fluzone® safely and effectively. See full prescribing information for Fluzone. Fluzone (Influenza Vaccine) injectable suspension, for intramuscular use 2025–2026 Formula Initial U.S. Approval: 198020260325