United States · FDA National Drug Code directory

Flucelvax

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
87063-299_5a564edc-83a3-1611-e063-6294a90a0b80
Product NDC
87063-299
Form
INJECTION, SUSPENSION
Composition / generic term
INFLUENZA A VIRUS A/Tasmania/318/2025 CVR-351 (H1N1) ANTIGEN (MDCK CELL DERIVED, PROPIOLACTONE INACTIVATED), INFLUENZA A VIRUS A/Tasmania/787/2025 CVR-388 (H3N2) ANTIGEN (MDCK CELL DERIVED, PROPIOLACTONE INACTIVATED), INFLUENZA B VIRUS B/Arizona/21/2025 ANTIGEN (MDCK CELL DERIVED, PROPIOLACTONE INACTIVATED)
Labeler
ASCLEMED USA INC.
Marketing category
BLA
Marketing start / end (source format)
20260701 / 20270731

Source-listed ingredients

  • INFLUENZA A VIRUS A/TASMANIA/318/2025 CVR-351 (H1N1) ANTIGEN (MDCK CELL DERIVED, PROPIOLACTONE INACTIVATED) — 15 ug/.5mL
  • INFLUENZA A VIRUS A/TASMANIA/787/2025 CVR-388 (H3N2) ANTIGEN (MDCK CELL DERIVED, PROPIOLACTONE INACTIVATED) — 15 ug/.5mL
  • INFLUENZA B VIRUS - B/ARIZONA/21/2025 ANTIGEN (MDCK CELL DERIVED, PROPIOLACTONE INACTIVATED) — 15 ug/.5mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 10 SYRINGE, GLASS in 1 CARTON (87063-299-10) / .5 mL in 1 SYRINGE, GLASS (87063-299-01) · 87063-299-10

Source and coverage

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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.

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