Modafinil

NDC 87063-307, Modafinil, tablet, from ASCLEMED USA INC..

Product NDC: 87063-307
Status: Listed
Labeler: ASCLEMED USA INC.
Dosage form: TABLET
Route: ORAL
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: ANDA
Application: ANDA202566
DEA schedule: CIV

Request

curl https://api.healthcare.dev/v1/drugs/ndc/87063-307 \
  -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 NDC	NDC-11	Package
87063-307-01	87063030701	100 TABLET in 1 BOTTLE (87063-307-01)
87063-307-30	87063030730	30 TABLET in 1 BOTTLE (87063-307-30)
87063-307-60	87063030760	60 TABLET in 1 BOTTLE (87063-307-60)
87063-307-90	87063030790	90 TABLET in 1 BOTTLE (87063-307-90)

Linked data

RxNorm, label and prices

RxNorm concepts

205324modafinil 200 MG Oral Tablet (SCD)

Related lookups

FDA label sections
GET /v1/drugs/labels/bfe1b1b7-52ec-41b3-94d6-ac56036eea80

Use it

Look up 87063-307 from code or an agent

curl

curl https://api.healthcare.dev/v1/drugs/ndc/87063-307 \
  -H "Authorization: Bearer $HDEV_API_KEY"

MCP prompt

Using the healthcare.dev MCP server, look up NDC 87063-307. 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.