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Zoledronic Acid

NDC 0143-9642, zoledronic acid, injection, solution, concentrate, from Hikma Pharmaceuticals USA Inc..

Product NDC
0143-9642
Status
Listed
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
INJECTION, SOLUTION, CONCENTRATE
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202182
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0143-9642 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ZOLEDRONIC ACID4 mg/5mL

Pharmacologic classes

Bisphosphonate [EPC]; Diphosphonates [CS]

Package NDCNDC-11Package
0143-9642-01001439642015 mL in 1 VIAL (0143-9642-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/784d33fa-0046-42eb-894b-3fc47dcfd4dc

Use it

Look up 0143-9642 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0143-9642 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0143-9642. 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.