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Primidone

NDC 80005-117, Primidone, tablet, from Carnegie Pharmaceuticals LLC.

Product NDC
80005-117
Status
Listed
Labeler
Carnegie Pharmaceuticals LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA218366
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/80005-117 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PRIMIDONE50 mg/1

Pharmacologic classes

Anti-epileptic Agent [EPC]; Decreased Central Nervous System Disorganized Electrical Activity [PE]

Package NDCNDC-11Package
80005-117-1180005011711100 TABLET in 1 BOTTLE (80005-117-11)
80005-117-1480005011714500 TABLET in 1 BOTTLE (80005-117-14)
80005-117-15800050117151000 TABLET in 1 BOTTLE (80005-117-15)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/dc018b1d-72d3-45a2-84ff-cf9499c7ae97

  • NADAC price for package 80005011711

    GET /v1/drugs/nadac/80005011711

  • NADAC price for package 80005011714

    GET /v1/drugs/nadac/80005011714

Use it

Look up 80005-117 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/80005-117 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 80005-117. 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.