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Goprelto

NDC 70839-359, cocaine hydrochloride, solution, from LXO US Inc..

Product NDC
70839-359
Status
Listed
Labeler
LXO US Inc.
Dosage form
SOLUTION
Route
NASAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA209963
DEA schedule
CII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70839-359 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • COCAINE HYDROCHLORIDE40 mg/mL
Package NDCNDC-11Package
70839-359-04708390359041 BOTTLE, GLASS in 1 CARTON (70839-359-04) / 4 mL in 1 BOTTLE, GLASS

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0f897764-fe30-090a-e063-6294a90af106

Use it

Look up 70839-359 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70839-359 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70839-359. 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.