NDC 0069-2501
Comirnaty 0.0158 mg per 0.48 mL injection, suspension
On the label: Pfizer Laboratories Div Pfizer Inc.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Pfizer Ireland Pharmaceuticals Unlimited Company | Dublin, Ireland | 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 |
| Pharmacia & Upjohn Company LLC | Kalamazoo, MI, United States | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyJun 16, 2023 · 9 inspections |
| Wyeth BioPharma Division of Wyeth Pharmaceuticals LLC | Andover, MA, United States | Makes the active ingredient and tests it | Problems found, fixed voluntarilyApr 8, 2026 · 5 inspections |
Product details
- Generic drug
- Bnt162b2 Omicron (lp.8.1): every company that makes it
- Form
- injection, suspension, intramuscular
- Strength
- 0.0158 mg per 0.48 mL
- Approval
- BLA BLA125742
- On the market since
- Aug 27, 2025
- Package NDCs
0069-2501-010069-2501-10- Official label
- DailyMed (National Library of Medicine), updated Sep 2, 2026
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