# Thiotepa

NDC: 0143-9565
Generic name: Thiotepa
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRACAVITARY, INTRAVENOUS, INTRAVESICAL
Marketing started: 20010601

FDA application: ANDA075547

## Active ingredients

- THIOTEPA: 15 mg/1.5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0143-9565"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0143-9565
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b19b03db-471d-4ee7-b1b8-6eccc39c41b0