68727-351 : Sunosi 150 mg Oral Tablet, Film Coated


NDC68727-351
Labeler: Jazz Pharmaceuticals, Inc.
Product Type: Human Prescription Drug
Drug Name:  Sunosi
Dosage Form: Oral Tablet, Film Coated
Application #: NDA211230
Rev. Date: 
CSA Schedule: CIV (US) [1]


[1] Schedule IV Controlled Substance: Low potential for abuse relative to substances in Schedule III. Examples include Alprazolam (Xanax), Diazepam (Valium), Carisoprodol (Soma), Clonazepam (Klonopin), Lorazepam (Ativan), Clorazepate (Tranxene), Midazolam (Versed), Temazepam (Restoril), and Triazolam (Halcion).. More Details: US Dept of Justice Controlled Substance Schedules.

NDC Package Codes:

  • 68727-351-01: 30 TABLET, FILM COATED IN 1 BOTTLE (68727‑351‑01)
  • 68727-351-02: 100 TABLET, FILM COATED IN 1 BOTTLE (68727‑351‑02)
  • 68727-351-07: 7 TABLET, FILM COATED IN 1 BLISTER PACK (68727‑351‑07)
  • 68727-351-10: 10 TABLET, FILM COATED IN 1 CARTON (68727‑351‑10)

Active Ingredients:

  • Solriamfetol

Dosage Strength:

  • 150 mg

Related Products:

Based on records with the same trade name.
  • 68727-350 Sunosi 75 mg Oral Tablet, Film Coated by Jazz Pharmaceuticals, Inc.

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