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RILUZOLE

NDC 69076-200, RILUZOLE, tablet, film coated, from Florida Pharmaceutical Products, LLC.

Product NDC
69076-200
Status
Listed
Labeler
Florida Pharmaceutical Products, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA206045
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69076-200 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • RILUZOLE50 mg/1

Pharmacologic classes

Benzothiazole [EPC]; Benzothiazoles [CS]

Package NDCNDC-11Package
69076-200-606907602006060 TABLET, FILM COATED in 1 BOTTLE (69076-200-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ccead445-970c-46a1-9532-2848cc2aa3b6

  • NADAC price for package 69076020060

    GET /v1/drugs/nadac/69076020060

Use it

Look up 69076-200 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69076-200 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69076-200. 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.