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Primidone

NDC 69584-685, Primidone, tablet, from Oxford Pharmaceuticals, LLC.

Product NDC
69584-685
Status
Listed
Labeler
Oxford Pharmaceuticals, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040586
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69584-685 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PRIMIDONE250 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
69584-685-1069584068510100 TABLET in 1 BOTTLE, PLASTIC (69584-685-10)
69584-685-5069584068550500 TABLET in 1 BOTTLE (69584-685-50)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/439096a4-c5d5-4ad8-be9c-238973a3e290

  • NADAC price for package 69584068510

    GET /v1/drugs/nadac/69584068510

  • NADAC price for package 69584068550

    GET /v1/drugs/nadac/69584068550

Use it

Look up 69584-685 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69584-685 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69584-685. 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.