# Docetaxel

NDC: 23155-905
Generic name: Docetaxel
Labeler / Manufacturer: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20241215

FDA application: ANDA216677

## Active ingredients

- DOCETAXEL: 160 mg/8mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"23155-905"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=23155-905
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=81686d37-a13f-46e2-b439-a84eb1433634