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Provigil

NDC 63459-201 · Cephalon, LLC

Generic nameModafinil

Dosage formTABLET

RouteORAL

Active ingredient(s)MODAFINIL

Strength200 mg/1

Pharmacologic classCentral Nervous System Stimulation [PE], Increased Sympathetic Activity [PE], Sympathomimetic-like Agent [EPC]

DEA scheduleCIV

Marketing categoryNDA

Packages

63459-201-30 — 30 TABLET in 1 BOTTLE (63459-201-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

57237-155 — Modafinil, 60429-009 — modafinil, 60429-010 — modafinil, 60505-2526 — modafinil, 60505-2527 — modafinil, 60505-4851 — Modafinil, 60505-4852 — Modafinil, 62332-385 — Modafinil, 62332-386 — Modafinil, 63459-101 — Modafinil, 63629-7315 — Modafinil, 65862-601 — Modafinil, 65862-602 — Modafinil, 68071-5121 — Modafinil, 68084-621 — Modafinil, 68084-721 — Modafinil, 68788-8280 — Modafinil, 68788-8653 — Modafinil, 69452-342 — Modafinil, 69452-343 — Modafinil, +32 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels