Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hospira, Inc. | Rocky Mount, NC, United States | Makes it, tests it, packages it and labels it | No problems foundFeb 7, 2025 · 11 inspections, 3 with FDA action |
| Hospira, Inc. | McPherson, KS, United States | Tests it | Problems found, fixed voluntarilyJan 17, 2025 · 16 inspections, 2 with FDA action |
Product details
- Generic drug
- Phytonadione: every company that makes it
- Form
- injection, emulsion, intramuscular; intravenous; subcutaneous
- Strength
- 2 mg per 1 mL
- Approval
- ANDA ANDA087954
- On the market since
- Jun 22, 2005
- Package NDCs
0409-9157-010409-9157-310409-9157-50- Official label
- DailyMed (National Library of Medicine), updated Aug 9, 2026
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