# Thiotepa

NDC: 43598-171
Generic name: Thiotepa
Labeler / Manufacturer: Dr.Reddy's Laboratories Inc.,
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRACAVITARY, INTRAVENOUS, INTRAVESICAL
Marketing started: 20221101

FDA application: ANDA214222

## Active ingredients

- THIOTEPA: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43598-171"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43598-171
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a8c8bb14-0423-e4a3-8bf0-8a66ce05b1bb