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 Inc | Chesterfield, MO, United States | Makes the active ingredient and tests it | No problems foundAug 20, 2019 · 4 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 |
| Pfizer Manufacturing Belgium NV | Puurs-Sint-Amands, Belgium | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyJun 22, 2022 · 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 Austria GmbH | Orth an der Donau, Austria | Tests it | Not inspected on record |
Product details
- Generic drug
- Meningococcal Groups A, B, C, W, and Y Vaccine: every company that makes it
- Form
- kit
- Strength
- 6 ingredients
- Approval
- BLA BLA125770
- On the market since
- Nov 27, 2023
- Package NDCs
0069-0271-010069-0332-010069-0600-010069-0600-050069-0600-100069-0600-99- Official label
- DailyMed (National Library of Medicine), updated Mar 17, 2026
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