24338-162 : Arynta 10 mg/ml Oral Solution


NDC: 24338-162
Labeler: Azurity Pharmaceuticals, Inc.
Product Type: Human Prescription Drug
Drug Name:  Arynta
Dosage Form: Oral Solution
Application #: NDA219847
Rev. Date: 
CSA Schedule: CII (US) [1]


[1] Schedule II / IIN Controlled Substance: High potential for abuse which may lead to severe psychological or physical dependence. (i.e. Narcotics such as Dilaudid, Methadone, Demerol, Oxycodone, Percocet, Fentanyl, Morphine, Opium, Codeine, and Hydrocodone ... Schedule IIN stimulants include non-narcotic Amphetamines such as Dexedrine, Adderall, Desoxyn, Methylphenidate (Ritalin) ... Other Schedule II substances include Amobarbital, Glutethimide, and Pentobarbital. More Details: US Dept of Justice Controlled Substance Schedules.

NDC Package Codes:

  • 24338-162-01: 1 BOTTLE IN 1 CARTON (24338‑162‑01) / 120 ML IN 1 BOTTLE

Active Ingredients:

  • Lisdexamfetamine Dimesylate

Dosage Strength:

  • 10 mg/mL

Pharmaceutical Classes:

  • Central Nervous System Stimulant [EPC]
  • Central Nervous System Stimulation [PE]

Related Products:

Based on records with the same trade name.
  • 24338-019 Arynta 10 mg/ml Oral Solution by Azurity Pharmaceuticals, Inc.
  • 24338-103 Arynta 10 mg/ml Oral Solution by Azurity Pharmaceuticals, Inc.
  • 24338-109 Arynta 10 mg/ml Oral Solution by Azurity Pharmaceuticals, Inc.
  • 24338-160 Arynta 10 mg/ml Oral Solution by Azurity Pharmaceuticals, Inc.

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