United States · FDA National Drug Code directory

mFLUSIVA

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
80777-500_3dd1c6d2-b054-4803-bb21-460b1b090d4c
Product NDC
80777-500
Form
INJECTION, SUSPENSION
Composition / generic term
Influenza Vaccine, mRNA
Labeler
Moderna US, Inc.
Marketing category
BLA
Marketing start / end (source format)
20260805
Source listing expiry
20271231

Source-listed ingredients

  • RNA-101-BFL3 — 12.5 ug/.38mL
  • RNA-101-BFL6 — 12.5 ug/.38mL
  • RNA-101-BFL5 — 12.5 ug/.38mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 10 SYRINGE, PLASTIC in 1 CARTON (80777-500-20) / .38 mL in 1 SYRINGE, PLASTIC (80777-500-18) · 80777-500-20

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.

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mFLUSIVA — United States | Molindra Medicines