17478-050 : Sufenta 50 ug/ml Intravenous Injection

NDC:	17478-050
Labeler:	Akorn
Product Type:	Human Prescription Drug
Drug Name:	Sufenta
Dosage Form:	Intravenous Injection
Application #:	NDA019050
Rev. Date:	Dec 1, 2010
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:

• 17478-050-01: 10 AMPULE IN 1 CARTON (17478‑050‑01) > 1 ML IN 1 AMPULE
• 17478-050-02: 10 AMPULE IN 1 CARTON (17478‑050‑02) > 2 ML IN 1 AMPULE
• 17478-050-05: 10 AMPULE IN 1 CARTON (17478‑050‑05) > 5 ML IN 1 AMPULE

Active Ingredients:

• Sufentanil Citrate

Pharmaceutical Classes:

• Full Opioid Agonists [MoA]
• Opioid Agonist [EPC]

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