NDC 81968-351 – Sunosi

Solriamfetol 150 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug DEA schedule CIV

Product NDC81968-351

Product details

Brand name
Sunosi
Generic name
Solriamfetol
Labeler
Axsome Therapeutics, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA211230
Marketed since
June 18, 2019
Listing expires
December 31, 2027
Pharmacologic class
Dopamine and Norepinephrine Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Sunosi →

Package NDC codes (3)

Package NDCDescriptionSince
81968-351-0130 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (81968-351-01)Jun 2, 2022
81968-351-07 sample7 TABLET, FILM COATED in 1 BLISTER PACK (81968-351-07)Jun 2, 2022
81968-351-10 sample10 BLISTER PACK in 1 CARTON (81968-351-10) / 7 TABLET, FILM COATED in 1 BLISTER PACK (81968-351-07)Jun 2, 2022

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