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Docetaxel

NDC 0955-1022, Docetaxel, injection, solution, concentrate, from Sanofi-Aventis U.S. LLC.

Product NDC
0955-1022
Status
Listed
Labeler
Sanofi-Aventis U.S. LLC
Dosage form
INJECTION, SOLUTION, CONCENTRATE
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA020449
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0955-1022 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DOCETAXEL160 mg/8mL

Pharmacologic classes

Microtubule Inhibition [PE]; Microtubule Inhibitor [EPC]

Package NDCNDC-11Package
0955-1022-08009551022081 VIAL, GLASS in 1 CARTON (0955-1022-08) / 8 mL in 1 VIAL, GLASS

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/dd0ca36d-1f54-4568-8d19-a7152addcd52

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=0955-1022

Use it

Look up 0955-1022 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0955-1022 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0955-1022. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.