# Thiotepa

NDC: 43598-650
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: 20180504

FDA application: ANDA210337

## Active ingredients

- THIOTEPA: 15 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43598-650"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43598-650
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0def6a5e-4bf5-b1fd-47b7-0f17ecfd9bc2