NDC 0093-3094 – Armodafinil

Armodafinil 250 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC0093-3094

Product details

Brand name
Armodafinil
Generic name
Armodafinil
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA021875
Marketed since
November 29, 2016
Marketing end
May 31, 2028

Active ingredients

Uses, dosage, side effects and warnings for Armodafinil →

Package NDC codes (1)

Package NDCDescriptionSince
0093-3094-5630 TABLET in 1 BOTTLE (0093-3094-56)Nov 29, 2016

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