NDC 0005-0100
Trumenba 60 ug per 0.5 mL injection, suspension
On the label: Wyeth Pharmaceutical Division of Wyeth Holdings LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Pfizer Health AB | Strangnas, Sweden | Makes the active ingredient and tests it | Problems found, fixed voluntarilyMar 6, 2026 · 6 inspections |
| Pfizer Ireland Pharmaceuticals Unlimited Company | Dublin, Ireland | Makes it, makes the active ingredient and tests it | Problems found, fixed voluntarilyDec 15, 2023 · 5 inspections |
| Wyeth Pharmaceutical Division of Wyeth Holdings LLC | Sanford, NC, United States | Makes the active ingredient and tests it | No problems foundFeb 28, 2011 · 1 inspection |
| Pfizer Manufacturing Belgium NV | Puurs-Sint-Amands, Belgium | Labels it | Problems found, fixed voluntarilyJun 22, 2022 · 5 inspections |
Product details
- Generic drug
- Neisseria Meningitidis Group B Recombinant Lp2086 A05 Protein Variant Antigen and Neisseria Meningitidis Group B Recombinant Lp2086 B01 Protein Variant Antigen: every company that makes it
- Form
- injection, suspension, intramuscular
- Strength
- 60 ug per 0.5 mL
- Approval
- BLA BLA125549
- On the market since
- Nov 5, 2014
- Package NDCs
0005-0100-010005-0100-050005-0100-10- Official label
- DailyMed (National Library of Medicine), updated Jan 19, 2026
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