# Docetaxel

NDC: 57884-3043
Generic name: Docetaxel
Labeler / Manufacturer: Jiangsu Hengrui Pharmaceuticals Co., Ltd.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION, CONCENTRATE
Routes: INTRAVENOUS
Marketing started: 20170809

FDA application: ANDA207252

## Active ingredients

- DOCETAXEL: 160 mg/8mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"57884-3043"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=57884-3043
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e488100d-6728-4f44-9282-f63a805b8e13