NDC 0143-9930
Cefotaxime 500 mg 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, tests it, packages it and labels it | Problems found, fixed voluntarilyApr 21, 2023 · 9 inspections, 1 with FDA action |
Product details
- Generic drug
- Cefotaxime: every company that makes it
- Form
- injection, powder, for solution, intramuscular; intravenous
- Strength
- 500 mg
- Approval
- ANDA ANDA065072
- On the market since
- Nov 20, 2002
- Package NDCs
0143-9930-010143-9930-10- Official label
- DailyMed (National Library of Medicine), updated Apr 11, 2024
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