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Modafinil

NDC 68788-8653, Modafinil, tablet, from Preferred Pharmaceuticals Inc..

Product NDC
68788-8653
Status
Listed
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207196
DEA schedule
CIV
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68788-8653 \
  -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
68788-8653-36878886530330 TABLET in 1 BOTTLE (68788-8653-3)
68788-8653-66878886530660 TABLET in 1 BOTTLE (68788-8653-6)
68788-8653-96878886530990 TABLET in 1 BOTTLE (68788-8653-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/60ec6e2a-2576-498f-9a8c-fddc53d4a44c

Use it

Look up 68788-8653 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-8653 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-8653. 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.