NDC 70771-1051 – Modafinil

Modafinil 100 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC70771-1051

Product details

Brand name
Modafinil
Generic name
Modafinil
Labeler
Zydus Lifesciences Limited
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA209966
Marketed since
January 4, 2018
Listing expires
December 31, 2026
Pharmacologic class
Sympathomimetic-like Agent

Active ingredients

Uses, dosage, side effects and warnings for Modafinil →

Package NDC codes (3)

Package NDCDescriptionSince
70771-1051-1100 TABLET in 1 BOTTLE (70771-1051-1)Jan 4, 2018
70771-1051-330 TABLET in 1 BOTTLE (70771-1051-3)Jan 4, 2018
70771-1051-990 TABLET in 1 BOTTLE (70771-1051-9)Jan 4, 2018

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