United States · FDA National Drug Code directory
FLULAVAL 2026/2027
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 19515-822_22a47299-7679-42e2-a61b-a8b6c12848f4
- Product NDC
- 19515-822
- Form
- SUSPENSION
- Composition / generic term
- influenza virus vaccine
- Labeler
- ID Biomedical Corporation of Quebec
- Marketing category
- BLA
- Marketing start / end (source format)
- 20260701 / 20270630
Source-listed ingredients
- INFLUENZA A VIRUS A/SWITZERLAND/6849/2025 IVR 278 (H1N1) ANTIGEN (UV, FORMALDEHYDE INACTIVATED) — 15 ug/.5mL
- INFLUENZA A VIRUS A/MICHIGAN/105/2025 SAN 049A (H3N2) ANTIGEN (UV, FORMALDEHYDE INACTIVATED) — 15 ug/.5mL
- INFLUENZA B VIRUS B/TOKYO/EIS13-175/2025 ANTIGEN (UV, FORMALDEHYDE INACTIVATED) — 15 ug/.5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 SYRINGE in 1 CARTON (19515-822-52) / .5 mL in 1 SYRINGE (19515-822-41) · 19515-822-52
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →