# Temsirolimus

NDC: 65219-200
Generic name: Temsirolimus
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: KIT
Routes: INTRAVENOUS
Marketing started: 20201120

FDA application: ANDA207383

## Active ingredients

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## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65219-200"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65219-200
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1c207bed-10e3-46f0-ad2c-69d5e5c97736