NDC 81968-351

SUNOSI

Solriamfetol

SUNOSI is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Axsome Therapeutics, Inc.. The primary component is Solriamfetol.

• Product ID: 81968-351_362f206b-73e7-4009-8c34-5a9df55679ab
• NDC: 81968-351
• Product Type: Human Prescription Drug
• Proprietary Name: SUNOSI
• Generic Name: Solriamfetol
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2019-06-18
• Marketing Category: NDA /
• Application Number: NDA211230
• Labeler Name: Axsome Therapeutics, Inc.
• Substance Name: SOLRIAMFETOL
• Active Ingredient Strength: 150 mg/1
• DEA Schedule: CIV
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 81968-351-01

1 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (81968-351-01)

• Marketing Start Date: 2022-06-02
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

NDC Crossover Matching brand name "SUNOSI" or generic name "Solriamfetol"

NDC	Brand Name	Generic Name
68727-350	SUNOSI	solriamfetol
68727-351	SUNOSI	solriamfetol
81968-350	SUNOSI	solriamfetol
81968-351	SUNOSI	solriamfetol