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BORTEZOMIB

NDC 70771-1708, BORTEZOMIB, injection, powder, lyophilized, for solution, from Zydus Lifesciences Limited.

Product NDC
70771-1708
Status
Listed
Labeler
Zydus Lifesciences Limited
Dosage form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route
INTRAVENOUS, SUBCUTANEOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA210204
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1708 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BORTEZOMIB1 mg/mL

Pharmacologic classes

Proteasome Inhibitor [EPC]; Proteasome Inhibitors [MoA]

Package NDCNDC-11Package
70771-1708-1707711708011 VIAL, SINGLE-DOSE in 1 CARTON (70771-1708-1) / 3.5 mL in 1 VIAL, SINGLE-DOSE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/582c7c0d-fa25-4586-8157-a1e2653d72d9

Use it

Look up 70771-1708 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1708 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70771-1708. 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.