67877-660 : Methadone Hydrochloride 10 mg Oral Tablet

NDC:	67877-660
Labeler:	Ascend Laboratories, LLC
Product Type:	Human Prescription Drug
Drug Name:	Methadone Hydrochloride
Dosage Form:	Oral Tablet
Application #:	ANDA090635
Rev. Date:	Aug 11, 2022
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:

• 67877-660-01: 100 TABLET IN 1 BOTTLE (67877‑660‑01)

Active Ingredients:

• Methadone Hydrochloride

Pharmaceutical Classes:

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

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