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ERIBULIN MESYLATE

NDC 70095-080, ERIBULIN MESYLATE, injection, from Sun Pharmaceutical Industries Limited.

Product NDC
70095-080
Status
Listed
Labeler
Sun Pharmaceutical Industries Limited
Dosage form
INJECTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA218743
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70095-080 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ERIBULIN MESYLATE.5 mg/mL

Pharmacologic classes

Microtubule Inhibition [PE]; Microtubule Inhibitor [EPC]

Package NDCNDC-11Package
70095-080-01700950080011 VIAL, SINGLE-DOSE in 1 CARTON (70095-080-01) / 2 mL in 1 VIAL, SINGLE-DOSE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2c0e145b-96b0-4f7b-8993-0f5f59afa81d

Use it

Look up 70095-080 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70095-080 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70095-080. 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.