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NDC 65219-029 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
| Labeler / Manufacturer | Fresenius Kabi USA, LLC |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA214222 |
| Dosage form / route | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRACAVITARY INTRAVENOUS INTRAVESICAL |
| Active ingredients | THIOTEPA (100 mg/1) |
| Marketing started | 20220411 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).