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Kit for the Preparation of Technetium Tc99m Mertiatide

NDC 45567-0655, Betiatide, injection, powder, lyophilized, for solution, from Sun Pharmaceutical Industries, Inc..

Product NDC
45567-0655
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208994
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/45567-0655 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BETIATIDE1 mg/1
Package NDCNDC-11Package
45567-0655-1455670655015 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 CARTON (45567-0655-1)

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0ad62039-f848-4f3d-b489-2524e6b6b86e

Use it

Look up 45567-0655 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/45567-0655 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 45567-0655. 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.