docetaxel
Generic: docetaxel
Labeler: hospira, inc.Drug Facts
Product Profile
Brand Name
docetaxel
Generic Name
docetaxel
Labeler
hospira, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
docetaxel 20 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0409-4235
Product ID
0409-4235_0eff97af-e2cd-46d7-84d3-0445a0910b1a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA022234
Listing Expiration
2026-12-31
Marketing Start
2021-06-28
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
04094235
Hyphenated Format
0409-4235
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
docetaxel (source: ndc)
Generic Name
docetaxel (source: ndc)
Application Number
NDA022234 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/mL
Packaging
- 1 VIAL, SINGLE-DOSE in 1 CARTON (0409-4235-01) / 1 mL in 1 VIAL, SINGLE-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "0eff97af-e2cd-46d7-84d3-0445a0910b1a", "openfda": {"unii": ["15H5577CQD"], "rxcui": ["1001405", "1860480"], "spl_set_id": ["6b9999bb-869e-4d25-838c-23c3ab280044"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (0409-4235-01) / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0409-4235-01", "marketing_start_date": "20210628"}], "brand_name": "Docetaxel", "product_id": "0409-4235_0eff97af-e2cd-46d7-84d3-0445a0910b1a", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Microtubule Inhibition [PE]", "Microtubule Inhibitor [EPC]"], "product_ndc": "0409-4235", "generic_name": "DOCETAXEL", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Docetaxel", "active_ingredients": [{"name": "DOCETAXEL", "strength": "20 mg/mL"}], "application_number": "NDA022234", "marketing_category": "NDA", "marketing_start_date": "20210628", "listing_expiration_date": "20261231"}