NDC 0143-9923
Cefazolin 225 mg per 1 mL injection, powder, for solution
On the label: Hikma Pharmaceuticals USA Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hikma Farmaceutica (portugal), S.a | Terrugem Sintra, Portugal | Makes it, packages it and labels it | Problems found, fixed voluntarilyApr 21, 2023 · 9 inspections, 1 with FDA action |
Product details
- Generic drug
- Cefazolin: every company that makes it
- Form
- injection, powder, for solution, intramuscular; intravenous
- Strength
- 225 mg per 1 mL
- Approval
- ANDA ANDA065047
- On the market since
- Sep 18, 2001
- Package NDCs
0143-9923-90- Official label
- DailyMed (National Library of Medicine), updated May 14, 2026
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