United States · FDA National Drug Code directory

Modafinil

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
55253-801_428b6de2-f791-43db-a186-d19312a348fd
Product NDC
55253-801
Form
TABLET
Composition / generic term
Modafinil
Labeler
CIMA LABS INC.
Marketing category
NDA AUTHORIZED GENERIC
Marketing start / end (source format)
20120329 / 20270331

Source-listed ingredients

  • MODAFINIL — 100 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET in 1 BOTTLE (55253-801-30) · 55253-801-30

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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