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Etomidate

NDC 68083-235, Etomidate Injection, solution, from Gland Pharma Limited.

Product NDC
68083-235
Status
Listed
Labeler
Gland Pharma Limited
Dosage form
SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209058
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68083-235 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ETOMIDATE2 mg/mL

Pharmacologic classes

General Anesthesia [PE]; General Anesthetic [EPC]

Package NDCNDC-11Package
68083-235-106808302351010 VIAL in 1 CARTON (68083-235-10) / 20 mL in 1 VIAL (68083-235-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/94cde4e7-3b46-419f-8dda-87675da8d89d

Use it

Look up 68083-235 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68083-235 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68083-235. 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.