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Ceftriaxone Sodium

NDC 67184-1005, Ceftriaxone Sodium, injection, powder, for solution, from Qilu Pharmaceutical Co., Ltd..

Product NDC
67184-1005
Status
Listed
Labeler
Qilu Pharmaceutical Co., Ltd.
Dosage form
INJECTION, POWDER, FOR SOLUTION
Route
INTRAMUSCULAR, INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203702
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/67184-1005 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CEFTRIAXONE SODIUM250 mg/1

Pharmacologic classes

Cephalosporin Antibacterial [EPC]; Cephalosporins [CS]

Package NDCNDC-11Package
67184-1005-16718410050110 VIAL, SINGLE-USE in 1 CARTON (67184-1005-1) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE
67184-1005-2671841005021 VIAL, SINGLE-USE in 1 CARTON (67184-1005-2) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4cdf0743-c62b-4969-b9c9-4c6400644f6c

Use it

Look up 67184-1005 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/67184-1005 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 67184-1005. 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.