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Lumryz

NDC 13551-005, sodium oxybate, kit, from Alkermes, Inc..

Product NDC
13551-005
Status
Listed
Labeler
Alkermes, Inc.
Dosage form
KIT
Route
—
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA214755
DEA schedule
CIII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/13551-005 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

None listed.

Package NDCNDC-11Package
13551-005-01135510005011 KIT in 1 CARTON (13551-005-01) * 1 FOR SUSPENSION, EXTENDED RELEASE in 1 PACKET * 1 FOR SUSPENSION, EXTENDED RELEASE in 1 PACKET * 1 FOR SUSPENSION, EXTENDED RELEASE in 1 PACKET

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/10e5e40c-52f3-4c73-8a34-2c29c690a934

Use it

Look up 13551-005 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/13551-005 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 13551-005. 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.