NDC 68084-721 – Modafinil

Modafinil 200 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC68084-721

Product details

Brand name
Modafinil
Generic name
Modafinil
Labeler
American Health Packaging
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202566
Marketed since
June 2, 2014
Listing expires
December 31, 2026
Pharmacologic class
Sympathomimetic-like Agent

Active ingredients

Uses, dosage, side effects and warnings for Modafinil →

Package NDC codes (1)

Package NDCDescriptionSince
68084-721-2130 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-721-21) / 1 TABLET in 1 BLISTER PACK (68084-721-11)Jun 2, 2014

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