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NDC 87333-090, Technetium Tc99m Generator, injection, solution, from SHINE SPECT USA, LLC.

Product NDC
87333-090
Status
Listed
Labeler
SHINE SPECT USA, LLC
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA017771
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/87333-090 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TECHNETIUM TC-99M SODIUM PERTECHNETATE250 mCi/mL
Package NDCNDC-11Package
87333-090-01873330090011 VIAL in 1 CARTON (87333-090-01) / 12 mL in 1 VIAL
87333-090-03873330090031 VIAL in 1 CARTON (87333-090-03) / 16 mL in 1 VIAL
87333-090-04873330090041 VIAL in 1 CARTON (87333-090-04) / 18 mL in 1 VIAL
87333-090-05873330090051 VIAL in 1 CARTON (87333-090-05) / 20 mL in 1 VIAL
87333-090-06873330090061 VIAL in 1 CARTON (87333-090-06) / 24 mL in 1 VIAL
87333-090-07873330090071 VIAL in 1 CARTON (87333-090-07) / 30 mL in 1 VIAL
87333-090-09873330090091 VIAL in 1 CARTON (87333-090-09) / 40 mL in 1 VIAL
87333-090-10873330090101 VIAL in 1 CARTON (87333-090-10) / 50 mL in 1 VIAL
87333-090-11873330090111 VIAL in 1 CARTON (87333-090-11) / 60 mL in 1 VIAL
87333-090-12873330090121 VIAL in 1 CARTON (87333-090-12) / 72 mL in 1 VIAL
87333-090-13873330090131 VIAL in 1 CARTON (87333-090-13) / 80 mL in 1 VIAL
87333-090-36873330090361 VIAL in 1 CARTON (87333-090-36) / 4 mL in 1 VIAL
87333-090-73873330090731 VIAL in 1 CARTON (87333-090-73) / 8 mL in 1 VIAL
87333-090-92873330090921 VIAL in 1 CARTON (87333-090-92) / 10 mL in 1 VIAL

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/626f10b5-cdbf-45b9-9cba-59a3c15f98bf

Use it

Look up 87333-090 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/87333-090 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 87333-090. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.