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Armodafinil

NDC 69339-180, Armodafinil, tablet, from Natco Pharma USA LLC.

Product NDC
69339-180
Status
Listed
Labeler
Natco Pharma USA LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202768
DEA schedule
CIV
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69339-180 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ARMODAFINIL250 mg/1
Package NDCNDC-11Package
69339-180-036933901800330 TABLET in 1 BOTTLE (69339-180-03)
69339-180-0569339018005500 TABLET in 1 BOTTLE (69339-180-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/de2f0921-e791-426c-9192-2b7162e2158c

Use it

Look up 69339-180 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69339-180 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69339-180. 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.