NDC 0068-0597
Rifadin IV 600 mg per 10 mL injection, powder, lyophilized, for solution
On the label: Sanofi-Aventis U.S. LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Euroapi Italy SRL | Brindisi, Italy | Makes the active ingredient and tests it | Serious problems, FDA actionJul 17, 2026 · 5 inspections, 1 with FDA action |
| Sanofi S.r.l. | Anagni, Italy | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyOct 29, 2024 · 7 inspections |
| Patheon Pharmaceuticals Inc. | Cincinnati, OH, United States | Tests it and packages it | Problems found, fixed voluntarilySep 26, 2025 · 15 inspections |
Product details
- Generic drug
- Rifampin: every company that makes it
- Form
- injection, powder, lyophilized, for solution
- Strength
- 600 mg per 10 mL
- Approval
- NDA NDA050627
- On the market since
- May 25, 1989
- Package NDCs
0068-0597-01- Official label
- DailyMed (National Library of Medicine), updated May 14, 2025
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