NDC 68788-7880 – Armodafinil

Armodafinil 150 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CIV

Product NDC68788-7880

Product details

Brand name
Armodafinil
Generic name
Armodafinil
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA206069
Marketed since
March 8, 2021
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Armodafinil →

Package NDC codes (3)

Package NDCDescriptionSince
68788-7880-330 TABLET in 1 BOTTLE (68788-7880-3)Mar 8, 2021
68788-7880-660 TABLET in 1 BOTTLE (68788-7880-6)Mar 8, 2021
68788-7880-990 TABLET in 1 BOTTLE (68788-7880-9)Mar 8, 2021

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