10191-1093 : Opium 30 [hp_c]/1 Sublingual Pellet


NDC10191-1093
Labeler: Remedy Makers
Product Type: Human Prescription Drug
Drug Name: Opium
Dosage Form: Sublingual Pellet
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:

  • 10191-1093-2: 137 PELLET IN 1 VIAL, GLASS (10191‑1093‑2)

Active Ingredients:

  • Opium

Dosage Strength:

  • 30 [hp_C]/1

Related Products:

Based on records with the same trade name.
  • 10191-1081 Opium 3 [hp_x]/1 Sublingual Pellet by Remedy Makers
  • 10191-1082 Opium 6 [hp_x]/1 Sublingual Pellet by Remedy Makers
  • 10191-1086 Opium 30 [hp_x]/1 Sublingual Pellet by Remedy Makers
  • 10191-1089 Opium 6 [hp_c]/1 Sublingual Pellet by Remedy Makers

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.