Modafinil

NDC 87063-308, Modafinil, tablet, from ASCLEMED USA INC..

Product NDC: 87063-308
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/87063-308 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

MODAFINIL100 mg/1

Pharmacologic classes

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

Package NDC	NDC-11	Package
87063-308-01	87063030801	100 TABLET in 1 BOTTLE (87063-308-01)
87063-308-30	87063030830	30 TABLET in 1 BOTTLE (87063-308-30)
87063-308-60	87063030860	60 TABLET in 1 BOTTLE (87063-308-60)
87063-308-90	87063030890	90 TABLET in 1 BOTTLE (87063-308-90)

Linked data

RxNorm, label and prices

RxNorm concepts

260218modafinil 100 MG Oral Tablet (SCD)

Related lookups

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

Use it

Look up 87063-308 from code or an agent

curl

curl https://api.healthcare.dev/v1/drugs/ndc/87063-308 \
  -H "Authorization: Bearer $HDEV_API_KEY"

MCP prompt

Using the healthcare.dev MCP server, look up NDC 87063-308. 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.