United States · FDA National Drug Code directory

Abrysvo

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
0069-2465_c3db32ba-8a3e-47d3-9dde-26a65f7bd0c0
Product NDC
0069-2465
Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Composition / generic term
Respiratory Syncytial Virus Vaccine
Labeler
Pfizer Laboratories Div Pfizer Inc
Marketing category
BLA
Marketing start / end (source format)
20240730
Source listing expiry
20271231

Source-listed ingredients

  • RECOMBINANT STABILIZED RSV A PREFUSION F ANTIGEN — .06 mg/.5mL
  • RECOMBINANT STABILIZED RSV B PREFUSION F ANTIGEN — .06 mg/.5mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 VIAL in 1 CARTON (0069-2465-01) / .5 mL in 1 VIAL (0069-2465-19) · 0069-2465-01
  • 10 VIAL in 1 CARTON (0069-2465-10) / .5 mL in 1 VIAL (0069-2465-19) · 0069-2465-10

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 →