42998-203 : Opium Tincture Deodorized 10 mg/ml Oral Solution

NDC:	42998-203
Labeler:	Marathon Pharmaceuticals, LLC
Product Type:	Human Prescription Drug
Drug Name:	Opium Tincture Deodorized
Dosage Form:	Oral Solution
Rev. Date:	Sep 17, 2008
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:

• 42998-203-01: 118.3 ML IN 1 BOTTLE, GLASS (42998‑203‑01)
• 42998-203-02: 473.2 ML IN 1 BOTTLE, GLASS (42998‑203‑02)

Active Ingredients:

• Morphine

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.

• 0187-4203 Opium Tincture Deodorized 10 mg/ml Oral Solution by Valeant Pharmaceuticals North America LLC
• 0574-0159 Opium Tincture Deodorized 10 mg/ml Oral Tincture by Paddock Laboratories, Inc.
• 42799-217 Opium Tincture Deodorized 10 mg/ml Oral Tincture by Edenbridge Pharmaceuticals, LLC
• 62559-153 Opium Tincture Deodorized 1 g/100ml Oral Solution by Anip Acquisition Company
• 63629-1965 Opium Tincture Deodorized 10 g/1000ml Oral Solution by Bryant Ranch Prepack

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