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Paclitaxel

NDC 68001-705, Paclitaxel, injection, from BluePoint Laboratories.

Product NDC
68001-705
Status
Listed
Labeler
BluePoint Laboratories
Dosage form
INJECTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216874
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68001-705 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PACLITAXEL6 mg/mL

Pharmacologic classes

Microtubule Inhibition [PE]; Microtubule Inhibitor [EPC]

Package NDCNDC-11Package
68001-705-27680010705271 VIAL, MULTI-DOSE in 1 CARTON (68001-705-27) / 50 mL in 1 VIAL, MULTI-DOSE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/59906bd2-8337-4cd8-9288-65b90eac2a7a

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=68001-705

Use it

Look up 68001-705 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68001-705 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68001-705. 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.