64950-359 : Goprelto 40 mg/ml Nasal Solution


NDC64950-359
Labeler: Genus Lifesciences Inc.
Product Type: Human Prescription Drug
Drug Name:  Goprelto
Dosage Form: Nasal Solution
Application #: NDA209963
Rev. Date: 
CSA Schedule: CII (US) [1]

NDC 64950-359 QR Code


[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:

  • 64950-359-04: 1 BOTTLE, GLASS IN 1 CARTON (64950‑359‑04) > 4 ML IN 1 BOTTLE, GLASS

Active Ingredients:

  • Cocaine Hydrochloride

Dosage Strength:

  • 40 mg/mL
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