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Docetaxel

NDC 47335-939, Docetaxel, injection, solution, from Sun Pharmaceutical Industries, Inc..

Product NDC
47335-939
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA022534
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/47335-939 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DOCETAXEL ANHYDROUS160 mg/8mL

Pharmacologic classes

Microtubule Inhibition [PE]; Microtubule Inhibitor [EPC]

Package NDCNDC-11Package
47335-939-40473350939401 VIAL, GLASS in 1 CARTON (47335-939-40) / 8 mL in 1 VIAL, GLASS

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c85b2c62-3c33-4cbc-8b79-d5e17851a1b4

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=47335-939

Use it

Look up 47335-939 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/47335-939 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 47335-939. 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.