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Docetaxel

NDC 0143-9205, Docetaxel, injection, solution, concentrate, from Hikma Pharmaceuticals USA Inc..

Product NDC
0143-9205
Status
Listed
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
INJECTION, SOLUTION, CONCENTRATE
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204490
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0143-9205 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DOCETAXEL20 mg/mL

Pharmacologic classes

Microtubule Inhibition [PE]; Microtubule Inhibitor [EPC]

Package NDCNDC-11Package
0143-9205-01001439205011 VIAL, GLASS in 1 CARTON (0143-9205-01) / 4 mL in 1 VIAL, GLASS

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ff7fb2c2-97a7-4716-a269-925ca30cf0f1

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=0143-9205

Use it

Look up 0143-9205 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0143-9205 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0143-9205. 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.