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POSLUMA

NDC 69932-002, flotufolastat F-18, injection, from Blue Earth Diagnostics.

Product NDC
69932-002
Status
Listed
Labeler
Blue Earth Diagnostics
Dosage form
INJECTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA216023
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69932-002 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FLOTUFOLASTAT F-18158 mCi/mL

Pharmacologic classes

Positron Emitting Activity [MoA]; Radioactive Diagnostic Agent [EPC]

Package NDCNDC-11Package
69932-002-506993200025025 mL in 1 VIAL, MULTI-DOSE (69932-002-50)

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/907ac4a4-a088-4826-ab50-cfc31985c9d4

Use it

Look up 69932-002 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69932-002 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69932-002. 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.