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IBANDRONATE SODIUM

NDC 62756-218, IBANDRONATE SODIUM, injection, solution, from Sun Pharmaceutical Industries, Inc..

Product NDC
62756-218
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090853
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/62756-218 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • IBANDRONATE SODIUM3 mg/3mL

Pharmacologic classes

Bisphosphonate [EPC]; Diphosphonates [CS]

Package NDCNDC-11Package
62756-218-40627560218401 VIAL, SINGLE-DOSE in 1 CARTON (62756-218-40) / 3 mL in 1 VIAL, SINGLE-DOSE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/be514be6-727a-4d6c-993b-52144f8e6de8

Use it

Look up 62756-218 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62756-218 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62756-218. 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.