NDC 0008-4990
Tygacil 50 mg per 5 mL injection, powder, lyophilized, for solution
On the label: Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Patheon Italia S.p.A. | Monza, Italy | Makes it, tests it and packages it | Problems found, fixed voluntarilyMay 26, 2023 · 10 inspections |
| Pfizer Ireland Pharmaceuticals Unlimited Company | Ringaskiddy, Ireland | Makes the active ingredient and tests it | Problems found, fixed voluntarilyOct 25, 2024 · 6 inspections |
| Wyeth Lederle SRL | Catania, Italy | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyNov 15, 2024 · 6 inspections, 2 with FDA action |
| Pharmacia & Upjohn Company LLC | Kalamazoo, MI, United States | Labels it | Problems found, fixed voluntarilyJun 16, 2023 · 9 inspections |
Product details
- Generic drug
- Tigecycline: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous
- Strength
- 50 mg per 5 mL
- Approval
- NDA NDA021821
- On the market since
- Jun 15, 2008
- Package NDCs
0008-4990-190008-4990-20- Official label
- DailyMed (National Library of Medicine), updated Nov 18, 2025
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