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Paclitaxel

NDC 0781-3531, Paclitaxel, injection, powder, lyophilized, for suspension, from Sandoz Inc.

Product NDC
0781-3531
Status
Listed
Labeler
Sandoz Inc
Dosage form
INJECTION, POWDER, LYOPHILIZED, FOR SUSPENSION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA212700
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0781-3531 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PACLITAXEL100 mg/20mL

Pharmacologic classes

Microtubule Inhibition [PE]; Microtubule Inhibitor [EPC]

Package NDCNDC-11Package
0781-3531-91007813531911 VIAL, SINGLE-DOSE in 1 CARTON (0781-3531-91) / 20 mL in 1 VIAL, SINGLE-DOSE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/15ca4829-8fee-45f9-b4bc-b31c15732cd6

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=0781-3531

Use it

Look up 0781-3531 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0781-3531 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0781-3531. 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.