NDC 70121-2749
Tepadina 200 mg injection, powder, lyophilized, for solution
On the label: Amneal Pharmaceuticals LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Adienne S.r.l. | Caponago, Italy | Makes it and tests it | Not inspected on record |
| Indena SpA | Settala, Italy | Makes the active ingredient and tests it | Problems found, fixed voluntarilyNov 26, 2021 · 8 inspections |
| Indena SpA | Milano, Italy | Makes the active ingredient | Problems found, fixed voluntarilyNov 26, 2021 · 8 inspections |
| Cit SRL | Burago Di Molgora, Italy | Packages it | Not inspected on record |
| Eurofins Biolab Srl | Vimodrone, Italy | Tests it | Problems found, fixed voluntarilySep 13, 2024 · 5 inspections |
| LabAnalysis Life Science srl | Casanova Lonati (PV), Italy | Tests it | Problems found, fixed voluntarilyJun 20, 2024 · 6 inspections, 1 with FDA action |
| NerPharMa S.r.l | Nerviano, Italy | Tests it | Problems found, fixed voluntarilySep 13, 2024 · 7 inspections |
Product details
- Generic drug
- Thiotepa: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intracavitary; intravenous; intravesical
- Strength
- 200 mg
- Approval
- NDA NDA208264
- On the market since
- Apr 18, 2025
- Package NDCs
70121-2749-1- Official label
- DailyMed (National Library of Medicine), updated Jan 30, 2026
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