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NITHIODOTE

NDC 60267-812, Sodium Nitrite and Sodium Thiosulfate, kit, from Hope Pharmaceuticals.

Product NDC
60267-812
Status
Listed
Labeler
Hope Pharmaceuticals
Dosage form
KIT
Route
—
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA201444
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/60267-812 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

None listed.

Package NDCNDC-11Package
60267-812-00602670812001 KIT in 1 CARTON (60267-812-00) * 10 mL in 1 VIAL, SINGLE-USE (60267-311-10) * 50 mL in 1 VIAL, SINGLE-DOSE (60267-705-50)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ff4941b3-9901-4aab-adcf-c5327bede34e

Use it

Look up 60267-812 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/60267-812 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 60267-812. 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.