NDC 71335-1308 – Armodafinil

Armodafinil 250 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC71335-1308

Product details

Brand name
Armodafinil
Generic name
Armodafinil
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA206069
Marketed since
March 6, 2018
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Armodafinil →

Package NDC codes (3)

Package NDCDescriptionSince
71335-1308-130 TABLET in 1 BOTTLE (71335-1308-1)Aug 23, 2019
71335-1308-228 TABLET in 1 BOTTLE (71335-1308-2)Aug 23, 2019
71335-1308-390 TABLET in 1 BOTTLE (71335-1308-3)Aug 23, 2019

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