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Modafinil

NDC 87063-309, Modafinil, tablet, from ASCLEMED USA INC..

Product NDC
87063-309
Status
Listed
Labeler
ASCLEMED USA INC.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209966
DEA schedule
CIV
Request
curl https://api.healthcare.dev/v1/drugs/ndc/87063-309 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MODAFINIL200 mg/1

Pharmacologic classes

Central Nervous System Stimulation [PE]; Increased Sympathetic Activity [PE]; Sympathomimetic-like Agent [EPC]

Package NDCNDC-11Package
87063-309-0187063030901100 TABLET in 1 BOTTLE (87063-309-01)
87063-309-308706303093030 TABLET in 1 BOTTLE (87063-309-30)
87063-309-608706303096060 TABLET in 1 BOTTLE (87063-309-60)
87063-309-908706303099090 TABLET in 1 BOTTLE (87063-309-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e88310cc-f356-4efa-9e61-9db583671904

Use it

Look up 87063-309 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/87063-309 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 87063-309. 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.