NDC 49281-645
Fluzone Trivalent Northern Hemisphere 15 ug per 0.5 mL injection, suspension
On the label: Sanofi Vaccines US Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Sanofi Vaccines US Inc. | Swiftwater, PA, United States | Makes it, packages it and labels it | Problems found, fixed voluntarilyApr 22, 2023 · 2 inspections |
Product details
- Generic drug
- Influenza A Virus A/Michigan/105/2025 San-049a (h3n2) Hemagglutinin Antigen (formaldehyde Inactivated) and Influenza A Virus A/Switzerland/6849/2025 Ivr-278 (h1n1) Hemagglutinin Antigen (formaldehyde Inactivated) and Influenza B Virus B/Tokyo/Eis13-175/2025 Hemagglutinin Antigen (formaldehyde Inactivated): every company that makes it
- Form
- injection, suspension, intramuscular
- Strength
- 15 ug per 0.5 mL
- Approval
- BLA BLA103914
- On the market since
- Jul 2, 2025
- Package NDCs
49281-645-1549281-645-78- Official label
- DailyMed (National Library of Medicine), updated Jun 29, 2026
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