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Bortezomib

NDC 70069-836, bortezomib, injection, powder, lyophilized, for solution, from Somerset Therapeutics LLC.

Product NDC
70069-836
Status
Listed
Labeler
Somerset Therapeutics LLC
Dosage form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route
INTRAVENOUS, SUBCUTANEOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211898
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70069-836 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BORTEZOMIB3.5 mg/3.5mL

Pharmacologic classes

Proteasome Inhibitor [EPC]; Proteasome Inhibitors [MoA]

Package NDCNDC-11Package
70069-836-01700690836011 VIAL in 1 CARTON (70069-836-01) / 3.5 mL in 1 VIAL

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/dc737d3d-2a4e-448a-ad70-e013065c411c

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=70069-836

Use it

Look up 70069-836 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70069-836 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70069-836. 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.