NDC 0143-9230
Rifampin 600 mg injection, powder, lyophilized, 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
- Rifampin: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous
- Strength
- 600 mg
- Approval
- ANDA ANDA205039
- On the market since
- Mar 3, 2016
- Package NDCs
0143-9230-01- Official label
- DailyMed (National Library of Medicine), updated Jan 28, 2022
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